Lediga jobb som Utvecklingschef i Uppsala

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Utvecklingshandledare till Arbete och Bostad i Uppsala

Ansök    Feb 18    Uppsala kommun    Utvecklingschef
Arbete och Bostad i Uppsala Just nu behöver vi på Arbete och bostad utöka vårt team med en utvecklingshandledare som är kommunikativ, som har lätt för att lyssna och anpassa sitt sätt att kommunicera. Vi söker framför allt dig som drivs av möjligheten att få jobba med kompetenta kollegor och gillar att arbeta med verksamhetsutveckling och Kommunikation. Känner du att det passar in på dig? Sök tjänsten redan idag! Välkommen till vård- och omsorgsförval... Visa mer
Arbete och Bostad i Uppsala

Just nu behöver vi på Arbete och bostad utöka vårt team med en utvecklingshandledare som är kommunikativ, som har lätt för att lyssna och anpassa sitt sätt att kommunicera. Vi söker framför allt dig som drivs av möjligheten att få jobba med kompetenta kollegor och gillar att arbeta med verksamhetsutveckling och Kommunikation. Känner du att det passar in på dig? Sök tjänsten redan idag!

Välkommen till vård- och omsorgsförvaltningen. Här arbetar vi med stöd och vård till äldre och till personer med funktionsnedsättning. Det handlar om öppna insatser, hemtjänst, korttidsvård, särskilt boende, LSS-verksamhet, personlig assistans, socialpsykiatri och hälso- och sjukvård. Målet är att äldre och personer med funktionsnedsättning ska kunna leva ett så aktivt och självständigt liv som möjligt.
Förvaltningen ansvarar också för biståndshandläggning, strategisk planering och upphandling och uppföljning.

Ditt uppdrag
I den här rollen ingår alternativ och kompletterande kommunikation (AKK). Kommunikation som ersätter eller kompletterar talat språk och kan fungera som ett stöd för personer som har svårt att använda eller förstå tal.

Din bakgrund
Till tjänsten som utvecklingshandledare söker vi dig som har akademisk utbildning eller annan utbildning som arbetsgivaren bedömer som relevant för tjänsten. Vidare kräver uppdraget att du har b-körkort. Det är meriterande om du har arbetat med Alternativ och kompletterande kommunikation.

Du har förmåga till helhetssyn och att se frågor i ett större perspektiv. Du är en kommunikativ person som har lätt för att lyssna och anpassa ditt sätt att kommunicera. Vidare är du en person som har en god pedagogisk förmåga och förståelse för människors olika förutsättningar att ta till sig kunskap. Du är bra på att strukturera, planera och prioritera ditt arbete.

Upplysningar
I Uppsala kommun värnar vi om varandras hälsa och arbetsmiljö. För att få arbeta brukarnära inom våra olika vård- och omsorgsverksamheter ska du vara vaccinerad mot Covid-19.

Har du frågor om tjänsten eller rekryteringsprocessen, kontakta:
Mats Jansson, utvecklingsledare, 018-727 23 19

Facklig företrädare:
Kommunal, Annika Öberg, 018-727 24 25

Har du frågor gällande registrering av din ansökan, kontakta enheten för kompetensförsörjning: 018-727 23 02.

I din ansökan ska du ange medborgarskap. Om du inte är medborgare i Sverige, EU, EES eller Schweiz måste du också kunna styrka att du har ett giltigt arbetstillstånd eller är undantagen från skyldigheten att ha arbetstillstånd. Anställning kan ske först efter kontroll av arbetstillstånd, vilket krävs enligt utlänningsförordningen.

Om vår organisation
Välkommen till vård- och omsorgsförvaltningen. Här arbetar vi med stöd och vård till äldre och till personer med funktionsnedsättning. Det handlar om öppna insatser, hemtjänst, korttidsvård, särskilt boende, LSS-verksamhet, personlig assistans, socialpsykiatri och hälso- och sjukvård. Målet är att äldre och personer med funktionsnedsättning ska kunna leva ett så aktivt och självständigt liv som möjligt. Förvaltningen ansvarar också för biståndshandläggning, strategisk planering, upphandling och uppföljning.

Mer information om vår organisation hittar du på uppsala.se (https://www.uppsala.se)
Undantagna (från heltid som norm) är personliga assistenter.
Vi undanber oss erbjudanden om annonserings- och rekryteringshjälp.

Dina personuppgifter kommer att användas för att administrera din ansökan inom Uppsala kommun. Visa mindre

Director of Operations

Ansök    Apr 4    Curval AB    Utvecklingschef
About this role: The Director of Operations is accountable for the operational performance of the business; delivering the financial plan; shaping and executing company strategy as well as developing the team and the site to meet future growth plans. Furthermore, the role will provide people leadership and act as Company Representative to internal and external stakeholders. The site operations include both delivery of customer projects based on our cutting... Visa mer
About this role:
The Director of Operations is accountable for the operational performance of the business; delivering the financial plan; shaping and executing company strategy as well as developing the team and the site to meet future growth plans. Furthermore, the role will provide people leadership and act as Company Representative to internal and external stakeholders.
The site operations include both delivery of customer projects based on our cutting-edge product portfolio and the development of new technologies as well as manufacturing of satellites and products and its supporting processes.
The Director will continue to grow the highly skilled team currently consisting of 30 persons with various engineering competencies to further deliver a revenue growth that last year exceeded 40%.
Responsibilities will include:
· Provide leadership of the site including load and capacity and organisational structure
· Accountable for all operational performance metrics (safety, quality, cost, people and delivery)
· Deliver the financial plan
· Company representative to external stakeholders and customers
· Setting strategic direction for the site
Skills Required:
· Financial and commercial acumen
· KPI Setting, delivery and management
· Ability to motivate the team and achieves goals through the work of others
· Professionalism and strong work ethic
· People Leadership skills
· Experience in product and production systems for space or other industrial applications
· Ability to interact with key internal and external stakeholders in country and globally
Why AAC Clyde Space
· A unique opportunity to become a part of shaping and growing one of the world leading companies in the fast-growing space industry
· Join, lead and develop a very highly skilled team of colleagues
· We are working on a daily basis to ensure that space technology works to the benefit of the Earth and space environment
This position is available to fill immediately, so applicants are encouraged to reply promptly with CV and covering letter.
As part of our recruitment process, we collect and process personal data relating to job applicants. We are committed to being transparent about how we collect and use this data, please click here to see our job applicant privacy notice.
For further information please contact Peter Ternebring, Recruiter, +46 70 639 88 89.
About AAC Clyde Space
AAC Clyde Space, a leading New Space company, specialises in small satellite technologies and services that enable businesses, governments, and educational organisations to access high-quality, timely data from space. This data has a vast range of applications, from weather forecasting to precision farming to environmental monitoring, and is essential to improving our quality of life on Earth.
Our growing capabilities bring together three divisions:
· Space Data as a Service – delivering data from space directly to customers
· Space missions – turnkey solutions that empower customers to streamline their space missions
· Space products and components – a full range of off-the-shelf and tailor-made subsystems, components, and sensors
AAC Clyde Space aims to become a world leader in commercial small satellites and services from space, applying advances in its technology to tackle global challenges and improve our life on Earth.
Some of our clients include Horizon Technologies, Orbcomm, NSLComm, OHB Sweden, Intuitive Machines, Orbital Micro Systems, the United States Airforce Academy, Swedish National Space Agency, UK Space Agency, European Space Agency and NASA.
AAC Clyde Space’s main operations are located in Sweden, the United Kingdom, the Netherlands, the USA and South Africa, with partner networks in Japan and South Korea. Visa mindre

Kvalitets- och utvecklingschef

Medborgarskolan är en ideell organisation som skapar mötesplatser för dig som söker kunskap, utveckling och upplevelser. Vår verksamhet inspirerar till lustfyllt och livslångt lärande. Våra kärnvärden är individen i centrum, utveckling i samverkan, ömsesidig respekt och kunskapens egenvärde. Medborgarskolan består av förbundskansliet, som är placerat i Uppsala, och åtta regioner. På förbundskansliet finns cirka 30 medarbetare. Medborgarskolan strävar ef... Visa mer
Medborgarskolan är en ideell organisation som skapar mötesplatser för dig som söker kunskap, utveckling och upplevelser. Vår verksamhet inspirerar till lustfyllt och livslångt lärande. Våra kärnvärden är individen i centrum, utveckling i samverkan, ömsesidig respekt och kunskapens egenvärde.

Medborgarskolan består av förbundskansliet, som är placerat i Uppsala, och åtta regioner. På förbundskansliet finns cirka 30 medarbetare.


Medborgarskolan strävar efter att alltid uppfylla och helst överträffa våra kunders och övriga intressenters förväntningar. Ett led i det arbetet är att vidareutveckla vårt systematiska kvalitetsarbete. Arbetet i kvalitetsfunktionen bedrivs i nära samarbete med regionerna.

Om tjänsten
Som kvalitets- och utvecklingschef leder du en grupp med fyra medarbetare och har personal- och budgetansvar. Du har ett coachande förhållningssätt och frigör potentialen hos dina medarbetare genom att skapa en arbetsmiljö med engagemang och motivation. Du drivs av utveckling och gillar förändring som möjliggör ny potential såväl för medarbetare som organisation. Du är en del av förbundskansliets ledningsgrupp.

I dina arbetsuppgifter ingår också att leda Medborgarskolans strategiska kvalitetsutveckling, vilket bland annat innebär att ansvara för utvecklingen av kvalitetsarbetet inom folkbildningsverksamheten och ansvara för och ge stöd åt arbetet med villkorad uppföljning av densamma. Vidare samordnar du nationella grupper, ger stöd åt och utvecklar utbildningar inom etik och kvalitetsområdet samt ansvarar för upprättande av rutiner inom kvalitetsledningssystemet.

Vi söker dig som är kommunikativ och genuint intresserad av att arbeta proaktivt, prestigelöst och i nära dialog med verksamheten. Du är drivande och självgående i ditt uppdrag och för att kunna driva arbetet framåt behöver du också vara målfokuserad och ha förmågan att både leda och inspirera andra. Du behöver kunna lyfta blicken och ha ett helhetsperspektiv över verksamheten. Som person är du strukturerad och noggrann.

Kvalifikationer
Du har för tjänsten relevant högskoleutbildning eller motsvarande som arbetsgivaren bedömer relevant, gärna också utbildning inom projektledning samt ledarskapsutbildning. Du har några års erfarenhet av att både projektleda och också operativt arbeta med verksamhetsutveckling kopplat till kvalitet inklusive villkors- och regelefterlevnad. Det är också meriterande om du har några års erfarenhet från arbete inom studieförbund eller annan idéburen verksamhet. Erfarenhet av verksamhet med offentlig finansiering samt av att ansöka om projektmedel är också ett plus. Du har en mycket god förmåga att uttrycka dig på svenska såväl i tal som i skrift.

Tjänsten är en 100 % tillsvidaretjänst med sex månaders provanställning och är placerad vid förbundskansliet i Uppsala. Medborgarskolan är en arbetsplats som värdesätter mångfald, vi välkomnar därför sökanden med olika bakgrund.

Om du har några frågor är du välkommen att höra av dig till Ann-Sofie Olding, förbundschef 018-569502 eller Marie Nyborg, HR 018-569539.

Välkommen med din ansökan senast 2022-03-27. Visa mindre

Utvecklingschef till Ledning förskola i Uppsala kommun

Ansök    Feb 4    Uppsala kommun    Utvecklingschef
Utbildningsförvaltningen, avdelning förskola Drivs du av ett starkt samhällsengagemang och vill vara med och skapa goda förutsättningar för barnen i Uppsala kommuns förskolor? Som utvecklingschef får du möjlighet samordna de utvecklingsinsatser som görs inom förskolan i Uppsala kommun. Vi söker dig som har erfarenhet av liknande uppdrag och som kan visa på goda resultat inom området! Välkommen med din ansökan! Ledning för kommunal förskola ansvarar för... Visa mer
Utbildningsförvaltningen, avdelning förskola

Drivs du av ett starkt samhällsengagemang och vill vara med och skapa goda förutsättningar för barnen i Uppsala kommuns förskolor? Som utvecklingschef får du möjlighet samordna de utvecklingsinsatser som görs inom förskolan i Uppsala kommun. Vi söker dig som har erfarenhet av liknande uppdrag och som kan visa på goda resultat inom området! Välkommen med din ansökan!

Ledning för kommunal förskola ansvarar för att driva, hålla samman och uppmuntra till utveckling på förskolorna. Ledningen skapar förutsättningar och följer upp rektorer och förskolornas arbete på ett övergripande plan.

Läs mer om vår verksamhet här: Förskola och familjedaghem (https://www.uppsala.se/skola-och-forskola/forskola-och-familjedaghem/)

Ditt uppdrag
Uppsala kommunala förskolor är en stor organisation. En så stor organisation behöver någon som håller ihop trådarna, en koordinator för ledningsgruppen och de utvecklingsinsatser som görs.
Vi samverkar med många aktörer, så som regionen, Uppsala universitet, andra förvaltningar, där uppgiften är att föra in det pedagogiska perspektivet och värna om förskolans särart. Ett bra samarbete med dessa aktörer är därför en viktig del i arbetet.

Som utvecklingschef driver och utvecklar du det systematiska kvalitetsarbetet tillsammans med våra verksamhetsutvecklare. Verksamhetsutvecklarna utvecklar stödbank, intranät, rutiner och allt som hör förskolorna till. Där har du en viktig samordnande funktion och är en länk mellan verksamhetsutvecklare och övriga ledningsgruppen.

Tjänsten är ny och du har i nuläget personalansvar för ett mindre antal medarbetare. Vi är också i en utvecklingsfas där vi ser över organiseringen av arbetsuppgifter och ansvarsområden inom Ledning förskola.

Du rapporterar till chefen för kommunal förskola och ingår i dennes ledningsgrupp. Som en del av ledningsgruppen är det viktigt att du dels stärker ledningsgruppen, men också att du kan företräda Uppsala kommun inom ditt område på ett professionellt sätt, samt att du är drivande och ansvarstagande i relation till dina egna avgränsade ansvarsområden.

Din bakgrund
Vi söker dig som drivs av ett starkt samhällsengagemang och vill vara med och skapa goda förutsättningar för barnen i Uppsala kommuns förskolor. Vi vill att du har erfarenhet av systematiskt kvalitetsarbete inom förskolan och har förskollärarutbildning eller lärarutbildning. Erfarenhet som förskollärare eller lärare är meriterande.

För att lyckas i uppdraget behöver du även ha:

• erfarenhet av att leda och driva processer
• erfarenhet och kunskaper inom analys av resultat och processer
• goda kunskaper om förskolans styrdokument och läroplan


Det är meriterande om du har:

• erfarenhet av liknande uppdrag som chef eller koordinator (eller motsvarande) inom förskolans ledningsorganisation
• erfarenhet som chef inom förskolan
• erfarenhet av förvaltningsövergripande arbete inom förskolan
• erfarenhet och kunskaper om den politiska processen i kommunal verksamhet


För att lyckas i detta uppdrag behöver du vara strategisk och ha god förmåga att se helheter och ta hänsyn till det större perspektivet. Att driva ditt arbete framåt mot resultat och ta initiativ till aktiviteter är något du trivs med och är bra på. Du kan ta beslut utifrån tillgänglig information och du agerar sedan tydligt utifrån besluten. Du kommunicerar med andra på ett lyhört och smidigt sätt, och du är bra på att skapa och utveckla goda relationer. Givetvis förstår du vikten av att anpassa din kommunikation i olika sammanhang och med olika personer. Vi vill också att du har lätt för att anpassa dig till ändrade förutsättningar och ser möjligheter i förändringar.

Upplysningar
I Uppsala kommun värnar vi om varandras hälsa och arbetsmiljö. Vi förväntar oss därför att du är vaccinerad mot Covid-19.

Har du frågor om tjänsten och rekryteringsprocessen är du välkommen att kontakta Jan Aili, chef kommunal förskola, 018-727 79 40, eller Hans Röllgårdh, HR-specialist, 018-727 22 83.

Fackliga företrädare:
Lärarförbundet, Louise Plobeck, 018-727 24 95
Vision, Maria Ros, 018-727 24 38
Akademikerförbundet SSR/SACO, Maria Persson, 018-727 24 24

I din ansökan ska du ange medborgarskap. Om du inte är medborgare i Sverige, EU, EES eller Schweiz måste du också kunna styrka att du har ett giltigt arbetstillstånd eller är undantagen från skyldigheten att ha arbetstillstånd. Anställning kan ske först efter kontroll av arbetstillstånd, vilket krävs enligt utlänningsförordningen.

Om vår organisation
Välkommen till utbildningsförvaltningen. Vi erbjuder förskola, grundskola och gymnasieskola för barn och ungdomar mellan 0 och 20 år. Tillsammans jobbar vi mot målet att alla elever ska nå bästa möjliga kunskapsresultat.

Mer information om vår organisation hittar du på uppsala.se (https://www.uppsala.se)
Vi undanber oss erbjudanden om annonserings- och rekryteringshjälp.

Dina personuppgifter kommer att användas för att administrera din ansökan inom Uppsala kommun. Visa mindre

Section Manager – Project Management Manufacturing

Ansök    Feb 4    Cytiva Sweden AB    Utvecklingschef
Be part of something altogether life-changing Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly... Visa mer
Be part of something altogether life-changing
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
We are now looking for a Section Manager – Project Management Manufacturing for the large-scale chemical & biological batch manufacturing. You will be a critical part of our Process & Digital Support team of 60 employees supporting the entire manufacturing at the Uppsala site. Do you have a passion for project execution and people development? Then we would love to hear from you.
What you’ll do
Be the direct manager for our team of excellent and experienced project leaders within manufacturing.
Develop and execute the strategy & operational plan for the section, including budget responsibility.
Coach and support individual project leaders in their continued personal development and refined project execution skills.
Secure project leaders for new product introductions, production development projects as well as digital manufacturing projects in accordance with business needs.
Review project progressions and ensure critical project milestones deliveries from a business and global supply chain perspective.
Ensure project to project lessons learnt and continuous improvements.

Who you are
Master’s degree in Chemical/Biotechnology/IT-engineering or equivalent relevant field.
Minimum 10 years of experience from Life Sciences industry.
Excellent skills at leading and developing people and teams.
Previous experience from project management.
Previous experience from a people leader position.
In order to succeed in this position, you need to be highly motivated, result-oriented, creative and with a strong collaborative attitude, focusing on both internal and external customer needs and the bigger picture.
Swedish and English both required as working languages

Our business is growing quickly and we hire across the board. Interview and selection will happen continuously. We look forward to hearing from you!
When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
If you’ve ever wondered what’s within you, there’s no better time to find out. Visa mindre

Clinical Trial Coordinator to Antaros Medical

Ansök    Jan 31    Antaros Medical AB    Utvecklingschef
Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading. At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) an... Visa mer
Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

To deliver on our commitments, we are looking for people with both broad and deep experience in clinical drug development as well as project management.

As a Clinical Trial Coordinator, you will be responsible for coordination in and administration of our clinical trials. The position will be located in our office in Uppsala.

Main responsibilities:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements).
- Attend project team meetings and generate meeting minutes.
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor


Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Collaboration skills in order to engage with people and clients
- Proven administrative skills
- Excellent knowledge of spoken and written Swedish and English


More information

For more information about the position, please contact Neha Mehta , +46 76-111-0659, or [email protected]

Please submit your application via this link with a short personal letter and your CV included, no later than February 10th 2022. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical
At Antaros Medical, we are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We currently have around 90 employees working at our offices in Mölndal and Uppsala. Visa mindre

Utvecklingsledare välfärdsbrott

Ansök    Jan 10    Uppsala kommun    Utvecklingschef
Trygghet, brottsförebyggande och säkerhet Trygghet, brottsförebyggande och säkerhet söker en utvecklingsledare välfärdsbrott. Bidragsfusk och olika brott mot välfärdssystemen kostar årligen samhället stora summor. Uppsala kommun arbetar därför aktivt mot välfärdsbrott i nära samverkan med polisen och flera statliga myndigheter och tar nu ett ytterligare steg för att stärka arbetet. Vill du ha ett omväxlande och meningsfullt arbete där du har möjlighet ... Visa mer
Trygghet, brottsförebyggande och säkerhet

Trygghet, brottsförebyggande och säkerhet söker en utvecklingsledare välfärdsbrott. Bidragsfusk och olika brott mot välfärdssystemen kostar årligen samhället stora summor. Uppsala kommun arbetar därför aktivt mot välfärdsbrott i nära samverkan med polisen och flera statliga myndigheter och tar nu ett ytterligare steg för att stärka arbetet.

Vill du ha ett omväxlande och meningsfullt arbete där du har möjlighet att bidra till att skapa ett tryggt och säkert samhälle? Då är jobbet inom Uppsala kommun något för dig. Vi vågar tänka stort, visa handlingskraft och med tillit låta nya idéer växa till hållbara lösningar.

Hos oss kommer du tillsammans med engagerade kollegor ges utvecklingsmöjligheter, samtidigt som ditt arbete bidrar till att öka tryggheten och minska brottsligheten inom kommunen och i tydliga och långsiktiga samarbeten mellan myndigheter. Enheten tar också fram beslutsunderlag, lägesbilder, rapporter, styrdokument, orsaksanalyser och utredningar inom trygghets- och säkerhetsområdet, samt verkar kunskapshöjande och stödjande för kommunens olika verksamheter genom, workshops, riskanalyser och vägledning. Enheten för trygghet, brottsförebyggande och säkerhet ansvarar även för personsäkerhet för kommunanställda och förtroendevalda samt ansvarar för kamerabevakning och ordningsvakter.

Läs mer om vår verksamhet här: Uppsala kommun (https://www.uppsala.se/)

Ditt uppdrag
Att arbeta som utvecklingsledare på enheten Trygghet, brottsförebyggande och säkerhet innebär i första hand att ansvara för det kommunövergripande arbetet kring välfärdsbrott genom att kartlägga, starta, utveckla samt samordna olika insatser och aktiviteter. Dessutom kommer du att ta nya initiativ, driva frågor framåt och presentera åtgärder, förslag och analyser inom området, samt omvärldsbevaka både internt och externt. Du kommer också aktivt att medverka och driva frågor inom enhetens övriga områden gällande trygghet, brottsförebyggande och säkerhetsarbete. Uppdraget omfattar både operativt och verksamhetsnära arbete samt strategisk planering.

Din bakgrund
Vi vänder oss till dig som har gedigen erfarenhet och bredd av såväl strategiskt arbete, som utredningsarbete mot ekonomisk och/eller organiserad brottslighet. Du har akademisk/högskoleutbildning och/eller annan utbildning som arbetsgivaren bedömer vara relevant för tjänsten. Alternativt annan utbildning i kombination med erfarenhet som arbetsgivaren bedömer relevant för tjänsten.
Du har även erfarenhet av att leda och samordna i komplexa uppdrag. Arbetet kräver även goda muntliga och skriftliga kunskaper i svenska, goda kunskaper i Office-paketet samt goda kunskaper i engelska. Det är meriterande om du har erfarenhet av arbete inom statlig myndighet eller kommun och arbete som utvecklingsledare eller har utbildning inom ledarskap.

Du har förmåga till helhetssyn och att se frågor i ett större perspektiv. Vidare är du kommunikativ och du har lätt för att lyssna och anpassa ditt sätt att kommunicera. Vi ser även att du är kreativ och ofta kommer med idéer och nya angreppssätt i arbetsrelaterade frågor. Sist men inte minst är du bra på att skapa, underhålla och utveckla arbetsmässiga relationer.

Upplysningar
I Uppsala kommun värnar vi om varandras hälsa och arbetsmiljö. Vi förväntar oss därför att du är vaccinerad mot Covid-19.

Har du frågor om tjänsten eller rekryteringsprocessen, kontakta:
Sofia Westring, enhetschef, 018-727 64 15

Fackliga företrädare:
Akavia, Jonny Eliasson, 018-727 22 12
Akademikerförbundet SSR, Maria Persson, 018-727 24 24


Har du frågor gällande registrering av din ansökan, kontakta enheten för kompetensförsörjning: 018-727 23 02.

Tjänsten är placerad i säkerhetsklass och säkerhetsprövning med registerkontroll kommer därför att genomföras före anställning.

I din ansökan ska du ange medborgarskap. Om du inte är medborgare i Sverige, EU, EES eller Schweiz måste du också kunna styrka att du har ett giltigt arbetstillstånd eller är undantagen från skyldigheten att ha arbetstillstånd. Anställning kan ske först efter kontroll av arbetstillstånd, vilket krävs enligt utlänningsförordningen.

Om vår organisation
Välkommen till kommunledningskontoret. Här jobbar du tillsammans med medarbetare på staber för kommunikation, HR, IT, ekonomi och fastighet samt avdelningarna kvalitet och planering, hållbarhet, trygghet, säkerhet och beredskap, kansli samt enheten för omvärld och ledningsstöd. På kommunledningskontoret ligger även organisationerna för näringsliv och destination samt gemensam service. Kommunledningskontoret är länken mellan våra förtroendevaldas beslut och kommunens alla verksamheter. Vårt uppdrag är bland annat att samordna och driva övergripande frågor inom demokrati, samhälls- och näringslivsutveckling samt ekologisk och social hållbarhet.

Mer information om vår organisation hittar du på uppsala.se (https://www.uppsala.se)
Vi undanber oss erbjudanden om annonserings- och rekryteringshjälp.

Dina personuppgifter kommer att användas för att administrera din ansökan inom Uppsala kommun. Visa mindre

Clinical Trial Coordinator to Antaros Medical

Ansök    Jan 11    Antaros Medical AB    Utvecklingschef
Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading. At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) an... Visa mer
Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

To deliver on our commitments, we are looking for people with both broad and deep experience in clinical drug development as well as project management.

As a Clinical Trial Coordinator, you will be responsible for coordination in and administration of our clinical trials. The position will be located in our office in Uppsala.

Main responsibilities:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements).
- Attend project team meetings and generate meeting minutes.
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor


Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Collaboration skills in order to engage with people and clients
- Proven administrative skills
- Excellent knowledge of spoken and written Swedish and English


More information

For more information about the position, please contact Neha Mehta , +46 76-111-0659, or [email protected]

Please submit your application via this link with a short personal letter and your CV included, no later than February 10th 2022. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical
At Antaros Medical, we are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We currently have around 90 employees working at our offices in Mölndal and Uppsala. Visa mindre

Software Developer to Antaros Medical

Ansök    Jan 11    Antaros Medical AB    Utvecklingschef
Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future? At Antaros Medical, we value competence and development as well as ideas and creativity. We are now looking for our next experienced Software Developer to join our development team in Malmö. As a Software Developer, you wil... Visa mer
Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future?

At Antaros Medical, we value competence and development as well as ideas and creativity. We are now looking for our next experienced Software Developer to join our development team in Malmö.

As a Software Developer, you will join a team of software developers and specialists in image processing and image analysis. You will be responsible for designing and developing tools for management, processing and analysis of medical MR and PET images acquired in clinical trials. You will also be member of cross-functional project teams in clinical trials, coordinating software development solutions in the project.

In addition, your work role will include software development support to specialists with rapid prototyping and implementation of method development in advanced image analysis.

Your main responsibilities will be:

- Development, maintenance and documentation of validated software for medical image management, processing, and analysis.

- Collaborate with cross-functional clinical trial teams to understand software needs and design and implement high quality solutions to problems.

- Continuous improvement of team processes and tools.

Who are we looking for?

We believe that you have been working with professional software development, preferably with medical images in a GxP or medical device setting, for at least 4 years. You are keen on working both independently as well as in teams, communicate well verbally and in writing and thrives in a fast-paced and dynamic environment. You can design and develop advanced yet simple solutions to complex problems in collaboration with other team members that fulfils industry standard quality requirements.

Requirements:

- 4+ years’ experience of professional software development

- B.Sc. degree in relevant field

- Python

- Experience in medical image processing

In addition, we perceive professional knowledge of DICOM, Matlab, C++, Deep learning and/or AWS, to be of advantage in the work role. Experience of GxP or medical device development is also meriting.

Are you interested?

Great to hear! Please submit your application via this link along with your CV included, no later than February 10th, 2022

For more information about the position, please contact Carl Sjöberg, Manager Software Development, [email protected] +46 73 050 04 69

The recruitment is for a permanent employment.

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialised in cardiorenal & metabolic diseases and oncology.

We combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. Visa mindre

Clinical Project Manager to Antaros Medical

Ansök    Jan 7    Antaros Medical AB    Utvecklingschef
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imagin... Visa mer
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than February 7, 2022

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected]

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Image Analyst to Antaros Medical

Ansök    Dec 27    Antaros Medical AB    Utvecklingschef
Are you interested in medical images and image analysis? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A company, where you would contribute and be a part of a collaborative team? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (P... Visa mer
Are you interested in medical images and image analysis? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A company, where you would contribute and be a part of a collaborative team? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing. As a part of our growth journey, we are looking for our next analytical and detail-focused Image Analyst to join our Corelab Team in Uppsala.

As an Image Analyst, you will be responsible for delivering high quality measurements and analyses of the imaging scans from MR and PET investigations, which is a core output from our company. You will work in a team that together analyses and delivers data for the clinical study. Your responsibility also includes quality control of such images and communication with imaging centres on image quality. The job environment is highly focused on research and technical development, and requires collaboration within the internal project team as well as with national and international clients and imaging centres.

Your main responsibilities will be:

- Quality control of the imaging scans and related documentation from the MR and PET investigations in the clinical trials
- Segmentation and analysis of the imaging scans from the MR and PET investigations including documentation
- Compiling results from image analysis and report back to clients according to agreed timelines
- Development, maintenance, and archiving of study documentation


Who are we looking for?

We emphasise personal suitability, and believe that you are a structured and thorough person with attention to details, who strives in an environment where high demands are placed on quality. We further believe that you are a service-oriented person who enjoys collaborating with others, as well as working individually.

We are happy to see that you have an interest in images, image analysis, technology and medicine.

Desired qualifications and skills:

- At least high school grade or equivalent, preferably in natural science. We perceive it as an advantage if you have university- or relevant higher education as biomedical scientist or similar.
- Demonstrated computer proficiency (programming skills are meritorious)
- Good knowledge of spoken and written Swedish and English


Understanding of and/or experience from working with clinical trials is considered an an advantage, including knowledge of ICH-GCP. We further perceive it as beneficial if you have skills and interest in programming.

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than January 31, 2022. Interviews can take place during the advertisement period.

For more information about the position, please contact Anna Ringheim Cadete, Corelab Manager, at +46 73 233 00 03 or [email protected]

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Clinical Project Manager to Antaros Medical

Ansök    Jan 10    Antaros Medical AB    Utvecklingschef
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imagin... Visa mer
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than February 7, 2022

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected]

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

MRI Radiographer/MR Imaging Specialist to Antaros Medical

Ansök    Dec 23    Antaros Medical AB    Utvecklingschef
Would you like to work as an MR Imaging Specialist in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PE... Visa mer
Would you like to work as an MR Imaging Specialist in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We currently have around 90 employees working at our offices in Sweden (Mölndal and Uppsala) and we are continuously growing and developing. As a part of our growth journey, we are now looking for an MR Imaging Specialist.

As an MR Imaging Specialist, you will be involved in the start-up and operational phase of clinical trials ensuring the best quality of MR images collected on the clinical imaging sites participating in our contract research studies and as part of our own R&D. Your main focus will be responsibility for setting up harmonized imaging protocols, training the sites on the procedures and communicating with imaging site staff.

You will join a group of imaging specialists with expertise in MR and PET, and you will be working closely with Imaging Scientists, Project Managers, and Image Analysts to deliver innovative imaging solutions to the pharmaceutical industry.

An important aspect of your job will be assuring image quality in clinical studies, including on-site and remote training and assessment of clinical imaging sites. You will be helping the imaging sites with the setting up of imaging protocols according to study requirements and educating them on the processes to be followed in the clinical trials that we work on.

Your main responsibilities will be:

- Managing imaging aspects of clinical trials
- Training and qualifying imaging sites


Requirements:

- A radiographer’s degree, specialization in MRI
- Extensive clinical MRI experience working as a radiographer or similar
- Experience in working with MRI scanners from multiple vendors
- Strong communication skills in English (written and oral)


Preferred qualifications:

- Experience in abdominal imaging
- Experience in working according to GCP and in clinical trials
- Experience in the pharmaceutical or medical technology industries




Who are we looking for?

We believe that you have strong organizational skills and drive your work independently, but enjoy working in project teams from start to finish to achieve the goal. You are comfortable communicating on the phone/Teams and e-mail.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

More information

For more information about the position, please contact Sofia Löwstedt, HR Director, at [email protected] or +46707158790.

Please submit your application via this link with a short personal letter and your CV included, no later than January 20, 2022.

The position is ideally based in our Uppsala or Mölndal office in Sweden but could possibly be placed internationally home-based in the US or Europe.

If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com)

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden. Visa mindre

Vi söker Chef Technology Transfer

Ansök    Dec 21    Fresenius Kabi AB    Utvecklingschef
Fresenius Kabi är ett globalt, marknadsledande företag specialiserat på klinisk nutrition, infusionsterapi och medicinsk teknik. Fresenius Kabi står för framsteg och kvalitet i utvecklingen av innovativa produkter och tjänster för terapi och vård av kroniskt och svårt sjuka människor - på och utanför sjukhus. Våra produkter och tjänster räddar och skyddar liv samt bidrar till att förbättra människors livskvalitet. Under mottot ”Caring for life” sätter ... Visa mer
Fresenius Kabi är ett globalt, marknadsledande företag specialiserat på klinisk nutrition, infusionsterapi och medicinsk teknik.

Fresenius Kabi står för framsteg och kvalitet i utvecklingen av innovativa produkter och tjänster för terapi och vård av kroniskt och svårt sjuka människor - på och utanför sjukhus. Våra produkter och tjänster räddar och skyddar liv samt bidrar till att förbättra människors livskvalitet.

Under mottot ”Caring for life” sätter Fresenius Kabi människan i centrum, som patient, kund och medarbetare.


Avdelningen Technology Transfer ett litet och viktigt team bestående av drivna och ambitiösa projektledare där du är med och driver utvecklingsprojekt från idé till industrialisering tillsammans med tredje part eller globala team inom Fresenius. Avdelningen ingår i Technical Operations där du kommer att tillhöra och verka i ledningsgruppen. Du tillsammans med din avdelning har en nyckelroll i den långsiktiga produktportföljen och har direktpåverkan på Fresenius Kabis framtid.

Arbetsuppgifter

Ge projektledare inom din avdelning och från andra delar av verksamheten rätt förutsättningar att följa projektprocesserna.
Mäta, visualisera och kontinuerligt förbättra projektprocesserna.
Regelbundet följa upp projektstatus och status för projektportföljen från idé till genomfört projekt.
Att leda och utveckla avdelningens arbete.
Om dig

Vi tror att du är ingenjör med lång erfarenhet av projektledning och projektportföljstyrning. Du har arbetat i chefspositioner tidigare och älskar att vara ledare. Erfarenhet av GMP är meriterande. Du talar och skriver flytande svenska och engelska.

För att bli framgångsrik som chef för Technology Transfer är du en person med ett tydligt ledarskap, starkt engagemang, driv och resultatfokus. Du är inte rädd för att fatta beslut och vill ständigt arbeta med utveckling. Du brinner för lagarbete, projektarbete och ser det som en utmaning att ta fram det bästa hos dina medarbetare.  Förtroende får du genom en öppen och ärlig dialog. Om du dessutom är analytisk och samarbetar väl över avdelningsgränserna så är du rätt person för tjänsten.

Om tjänsten

Tjänsten är en visstidsanställning i prövosyfte som efter 6 månader övergår i tillsvidareanställning efter överenskommelse. Tillträde omgående. Placeringsort är Uppsala.

Om oss

Vi är ett växande företag med cirka 1100 anställda i Sverige, och över 37 000 anställda världen över. Vi är stolta över våra produkter och det genomsyrar hela företaget. I våra medarbetarundersökningar lyfts kollegorna, utvecklingsmöjligheterna och den familjära stämningen upp som några av de bästa sakerna med att arbeta på Fresenius Kabi.

Att vara en del i Fresenius Kabi är synonymt med att vara en del i en miljö med framtidsutsikter. Vi tror på vår personal och är passionerad i vår utveckling av alla våra medarbetare. Vår världsomfattande utsträckning innebär att där finns en stor variation av vägar att välja som ett led i din framtida utveckling.

Kontakt

Vill du veta mer om tjänsten är du välkommen att kontakta Aram Yildiz 018–644 250. Fackliga kontaktpersoner är Frank Glackin för Unionen, 018–644 773 och Linda Holm för SACO, 018–644 195.

Välkommen med din ansökan via länken nedan, urval och rekrytering kan komma att ske löpande. Vi tar inte emot ansökningar via e-mail eller post Visa mindre

Software Developer to Antaros Medical

Ansök    Dec 10    Antaros Medical AB    Utvecklingschef
Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future? At Antaros Medical, we value competence and development as well as ideas and creativity. We are now looking for our next experienced Software Developer to join our development team in Malmö. As a Software Developer, you wil... Visa mer
Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future?

At Antaros Medical, we value competence and development as well as ideas and creativity. We are now looking for our next experienced Software Developer to join our development team in Malmö.

As a Software Developer, you will join a team of software developers and specialists in image processing and image analysis. You will be responsible for designing and developing tools for management, processing and analysis of medical MR and PET images acquired in clinical trials. You will also be member of cross-functional project teams in clinical trials, coordinating software development solutions in the project.

In addition, your work role will include software development support to specialists with rapid prototyping and implementation of method development in advanced image analysis.

Your main responsibilities will be:

- Development, maintenance and documentation of validated software for medical image management, processing, and analysis.

- Collaborate with cross-functional clinical trial teams to understand software needs and design and implement high quality solutions to problems.

- Continuous improvement of team processes and tools.

Who are we looking for?

We believe that you have been working with professional software development, preferably with medical images in a GxP or medical device setting, for at least 4 years. You are keen on working both independently as well as in teams, communicate well verbally and in writing and thrives in a fast-paced and dynamic environment. You can design and develop advanced yet simple solutions to complex problems in collaboration with other team members that fulfils industry standard quality requirements.

Requirements:

- 4+ years’ experience of professional software development

- B.Sc. degree in relevant field

- Python

- Experience in medical image processing

In addition, we perceive professional knowledge of DICOM, Matlab, C++, Deep learning and/or AWS, to be of advantage in the work role. Experience of GxP or medical device development is also meriting.

Are you interested?

Great to hear! Please submit your application via this link along with your CV included, no later than January 10th, 2022

For more information about the position, please contact Carl Sjöberg, Manager Software Development, [email protected] +46 73 050 04 69

The recruitment is for a permanent employment.

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialised in cardiorenal & metabolic diseases and oncology.

We combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. Visa mindre

Vi söker en Global Regulatory Affairs Manager

Ansök    Nov 30    Fresenius Kabi AB    Utvecklingschef
Fresenius Kabi är ett globalt, marknadsledande företag specialiserat på klinisk nutrition, infusionsterapi och medicinsk teknik. Fresenius Kabi står för framsteg och kvalitet i utvecklingen av innovativa produkter och tjänster för terapi och vård av kroniskt och svårt sjuka människor - på och utanför sjukhus. Våra produkter och tjänster räddar och skyddar liv samt bidrar till att förbättra människors livskvalitet. Under mottot ”Caring for life” sätter ... Visa mer
Fresenius Kabi är ett globalt, marknadsledande företag specialiserat på klinisk nutrition, infusionsterapi och medicinsk teknik.

Fresenius Kabi står för framsteg och kvalitet i utvecklingen av innovativa produkter och tjänster för terapi och vård av kroniskt och svårt sjuka människor - på och utanför sjukhus. Våra produkter och tjänster räddar och skyddar liv samt bidrar till att förbättra människors livskvalitet.

Under mottot ”Caring for life” sätter Fresenius Kabi människan i centrum, som patient, kund och medarbetare.


Vill du jobba för en global marknadsledare med en komplett produktportfölj för kritiskt sjuka patienter?

Fresenius Kabi söker en Global Regulatory Affairs Manager till den regulatoriska avdelningen inom affärsenheten Parenteral Nutrition, Keto-Analogues and Standard I.V. Fluids.

Om oss

Affärsenheten Parenteral Nutrition, Keto-Analogues and Standard I.V. Fluids ansvarar för en global portfölj av läkemedelsprodukter. Ansvarsområden inkluderar produktion, produktutveckling samt fortlöpande livscykelhantering vilket omfattar strategier för produktportföljen, lönsamhetsberäkningar, strategisk planering och dess verkställande. Vi ansvarar även för produktpositionering genom kommunikation, marknadsföring och globala marknadsföringskampanjer. Vidare supporterar vi regionala och nationella marknadsbolag med vetenskapligt stöd.

Regulatory Affairs har en central roll i upprätthållandet av marknadsföringstillstånd för den globala produktportföljen men även i utvecklingsarbetet av nya produkter.

Din roll

Som Regulatory Affairs Manager kommer du ansvara för att planera och samordna regulatoriska aktiviteter inom EU, främst ändringsärenden (MRP), men även förnyelseansökningar, PSUSor och nyansökningar (MRP/DCP) förekommer. 

Du ansvarar för att sammanställa underlaget och utvärdera dokumentationen som behövs för godkännande av nya produkter, förnyelseansökningar och ändringsärenden ur ett globalt perspektiv. Detta görs i nära samarbete med olika expertfunktioner inom företaget, marknadsbolagen samt kollegor på den regulatoriska avdelningen.

En del av arbetet sker i projektform med internationella kontakter.

Genomgående för din position är även den koordinerande rollen där interna funktioner och nationella och centrala myndigheter utgör kontaktytor och förutsättningen för en framgångsrik planering, prioritering och genomförande av regulatoriska aktiviteter.

Arbetet innebär en stimulerande mix av rutinärenden blandat med regulatoriska utmaningar. Det är en bred, spännande och dynamisk roll som inkluderar dagliga kontakter med kollegor över hela världen.

Din profil

Du som söker har naturvetenskaplig högskoleutbildning, gärna farmaceutisk eller motsvarande. Du har med fördel minst 5 års regulatorisk erfarenhet ifrån läkemedelsindustri eller myndigheter med tillämpade kunskaper om relevanta föreskrifter och riktlinjer inom området. Du har mycket goda kunskaper i engelska och svenska, i både tal och skrift. Du är utåtriktad och tar för dig även i globala sammanhang. Som person är du självständig och stabil, har lätt att samarbeta, är drivande och inriktad på att nå resultat och lösa problem.

Att vara en del i Fresenius Kabi är synonymt med att vara en del i en miljö med framtidsutsikter. Vi tror på vår personal och är passionerad i vår utveckling av alla våra medarbetare. Hur den utvecklingen ser ut har du stora möjligheter att påverka själv. Vår globala organisation medför att det finns en stor variation av vägar att välja som ett led i din framtida utveckling.

Om tjänsten

Tjänsten är en visstidsanställning i prövosyfte som efter 6 månader övergår i tillsvidareanställning efter överenskommelse mellan parterna.

Tillträde omgående. Tjänsten är baserad i Uppsala.

Om företaget

Fresenius Kabi är ett globalt, marknadsledande företag specialiserat på klinisk nutrition, infusionsterapi och medicinsk teknik.
Fresenius Kabi står för framsteg och kvalitet i utvecklingen av innovativa produkter och tjänster för terapi och vård av kroniskt och svårt sjuka människor - på och utanför sjukhus. Deras produkter och tjänster räddar och skyddar liv samt bidrar till att förbättra människors livskvalitet.
Under mottot ”Caring for life” sätter Fresenius Kabi människan i centrum, som patient, kund och medarbetare.

Kontakt

Vill du veta mer om tjänsten är du välkommen att kontakta Jens Funestad, 018–644 299. Fackliga kontaktpersoner är Frank Glackin för Unionen, 018–644 773 och Linda Holm för Akademikerföreningen, 018–644 195.  

Välkommen med din ansökan via länken nedan, urval och rekrytering kan komma att ske löpande. Sista ansökningsdag 2021-12-12.

Vi tar inte emot ansökningar via e-mail eller post. Visa mindre

Clinical Trial Coordinator to Antaros Medical

Ansök    Dec 10    Antaros Medical AB    Utvecklingschef
Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading. At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) an... Visa mer
Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

To deliver on our commitments, we are looking for people with both broad and deep experience in clinical drug development as well as project management.

As a Clinical Trial Coordinator, you will be responsible for coordination in and administration of our clinical trials. The position will be located in our office in Uppsala.

Main responsibilities:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements).
- Attend project team meetings and generate meeting minutes.
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor


Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Collaboration skills in order to engage with people and clients
- Proven administrative skills
- Excellent knowledge of spoken and written Swedish and English


More information

For more information about the position, please contact Neha Mehta , +46 76-111-0659, or [email protected]

Please submit your application via this link with a short personal letter and your CV included, no later than January 10th 2022. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical
At Antaros Medical, we are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We currently have around 90 employees working at our offices in Mölndal and Uppsala. Visa mindre

Clinical Project Manager to Antaros Medical

Ansök    Dec 6    Antaros Medical AB    Utvecklingschef
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imagin... Visa mer
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than December 31st, 2021.

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected]

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Clinical Project Manager to Antaros Medical

Ansök    Nov 9    Antaros Medical AB    Utvecklingschef
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imagin... Visa mer
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than November 30th, 2021.

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected]

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Clinical Trial Coordinator to Antaros Medical

Ansök    Okt 1    Antaros Medical AB    Utvecklingschef
Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading. At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) an... Visa mer
Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

To deliver on our commitments, we are looking for people with both broad and deep experience in clinical drug development as well as project management.

As a Clinical Trial Coordinator, you will be responsible for coordination in and administration of our clinical trials. The role may also include overall administrative support in driving our business forward. The position will be located in our office in Uppsala or Mölndal.

Main responsibilities:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements).
- Attend project team meetings and generate meeting minutes.
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor


Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Collaboration skills in order to engage with people and clients
- Proven administrative skills
- Excellent knowledge of spoken and written Swedish and English


More information

For more information about the position, please contact Neha Mehta , +46 76-111-0659, or [email protected]

Please submit your application via this link with a short personal letter and your CV included, no later than October 31, 2021. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical
At Antaros Medical, we are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We currently have around 90 employees working at our offices in Mölndal and Uppsala. Visa mindre

Software Developer to Antaros Medical

Ansök    Nov 9    Antaros Medical AB    Utvecklingschef
Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future? At Antaros Medical, we value competence and development as well as ideas and creativity. We are now looking for our next experienced Software Developer to join our development team in Uppsala. As a Software Developer, you w... Visa mer
Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future?

At Antaros Medical, we value competence and development as well as ideas and creativity. We are now looking for our next experienced Software Developer to join our development team in Uppsala.

As a Software Developer, you will join a team of software developers and specialists in image processing and image analysis. You will be responsible for designing and developing tools for management, processing and analysis of medical MR and PET images acquired in clinical trials. You will also be member of cross-functional project teams in clinical trials, coordinating software development solutions in the project.

In addition, your work role will include software development support to specialists with rapid prototyping and implementation of method development in advanced image analysis.

Your main responsibilities will be:

- Development, maintenance and documentation of validated software for medical image management, processing, and analysis.

- Collaborate with cross-functional clinical trial teams to understand software needs and design and implement high quality solutions to problems.

- Continuous improvement of team processes and tools.

Who are we looking for?

We believe that you have been working with professional software development, preferably with medical images in a GxP or medical device setting, for at least 4 years. You are keen on working both independently as well as in teams, communicate well verbally and in writing and thrives in a fast-paced and dynamic environment. You can design and develop advanced yet simple solutions to complex problems in collaboration with other team members that fulfils industry standard quality requirements.

Requirements:

- 4+ years’ experience of professional software development

- B.Sc. degree in relevant field

- Python

- Experience in medical image processing

In addition, we perceive professional knowledge of DICOM, Matlab, C++, Deep learning and/or AWS, to be of advantage in the work role. Experience of GxP or medical device development is also meriting.

Are you interested?

Great to hear! Please submit your application via this link along with your CV included, no later than November 30, 2021.

For more information about the position, please contact Carl Sjöberg, Manager Software Development, [email protected] +46 73 050 04 69

The recruitment is for a permanent employment.

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialised in cardiorenal & metabolic diseases and oncology.

We combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. Visa mindre

Image Analyst to Antaros Medical

Ansök    Okt 1    Antaros Medical AB    Utvecklingschef
Are you interested in medical images and image analysis? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A company, where you would contribute and be a part of a collaborative team? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (P... Visa mer
Are you interested in medical images and image analysis? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A company, where you would contribute and be a part of a collaborative team? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing. As a part of our growth journey, we are looking for our next analytical and detail-focused Image Analyst to join our Corelab Team in Uppsala.

As an Image Analyst, you will be responsible for delivering high quality measurements and analyses of the imaging scans from MR and PET investigations, which is a core output from our company. You will work in a team that together analyses and delivers data for the clinical study. Your responsibility also includes quality control of such images and communication with imaging centres on image quality. The job environment is highly focused on research and technical development, and requires collaboration within the internal project team as well as with national and international clients and imaging centres.

Your main responsibilities will be:

- Quality control of the imaging scans and related documentation from the MR and PET investigations in the clinical trials
- Segmentation and analysis of the imaging scans from the MR and PET investigations including documentation
- Compiling results from image analysis and report back to clients according to agreed timelines
- Development, maintenance, and archiving of study documentation


Who are we looking for?

We emphasise personal suitability, and believe that you are a structured and thorough person with attention to details, who strives in an environment where high demands are placed on quality. We further believe that you are a service-oriented person who enjoys collaborating with others, as well as working individually.

We are happy to see that you have an interest in images, image analysis, technology and medicine.

Desired qualifications and skills:

- At least high school grade or equivalent, preferably in natural science. We perceive it as an advantage if you have university- or relevant higher education as biomedical scientist or similar.
- Demonstrated computer proficiency (programming skills are meritorious)
- Good knowledge of spoken and written Swedish and English


Understanding of and/or experience from working with clinical trials is considered an an advantage, including knowledge of ICH-GCP. We further perceive it as beneficial if you have skills and interest in programming.

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than October 31, 2021. Interviews can take place during the advertisement period.

For more information about the position, please contact Anna Ringheim Cadete, Corelab Manager, at +46 73 233 00 03 or [email protected]

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Bildanalytiker till Antaros Medical

Ansök    Sep 30    Antaros Medical AB    Utvecklingschef
Har du intresse av bilder och bildanalys? Vill du jobba på ett företag som gör skillnad inom läkemedelsutveckling, på en arbetsplats där du får vara en del av ett sammansvetsat team? Då har vi en intressant tjänst för dig. Antaros Medical utvecklar nya metoder inom imaging samt analyserar bilder från MRI- och PET-undersökningar från kliniska prövningar, med specialisering inom kardiometabola sjukdomar och onkologi. Vi har ett globalt nätverk av partners o... Visa mer
Har du intresse av bilder och bildanalys? Vill du jobba på ett företag som gör skillnad inom läkemedelsutveckling, på en arbetsplats där du får vara en del av ett sammansvetsat team? Då har vi en intressant tjänst för dig.

Antaros Medical utvecklar nya metoder inom imaging samt analyserar bilder från MRI- och PET-undersökningar från kliniska prövningar, med specialisering inom kardiometabola sjukdomar och onkologi. Vi har ett globalt nätverk av partners och kunder, både stora och små läkemedelsföretag, och deltar även i flera europeiska forskningssamarbeten. Vi är ett snabbt växande företag och har för närvarande cirka 90 anställda baserade i BioVentureHub i Mölndal och i Uppsala Science Park. Nyligen öppnade vi ett kontor i USA.

Vi söker nu en analytisk och detaljfokuserad Bildanalytiker (Image Analyst) som vill vara med och bidra på vår resa. Som bildanalytiker på Antaros Medical arbetar du med kvalitetskontroll och högkvalitativa mätningar och analyser av bilder från MR- och PET-undersökningar i en teknisk och forskningsintensiv miljö. Du kommer att arbeta i ett team som tillsammans levererar data för den kliniska studien och ha kontakt med nationella och internationella kunder och imaging-center/röntgenkliniker. Tjänsten är placerad på vårt kontor i Uppsala.

Din profil

Vi lägger stor vikt vid personlig lämplighet, och tror att du är en strukturerad och noggrann person som trivs i en miljö där höga krav ställs på vårt kvalitetsarbete. Vidare tror vi att du är en serviceinriktad person som trivs i samarbete med andra såväl som att arbeta individuellt. Vi ser gärna att du har ett intresse för bilder, bildananalys, teknik och medicin.

Utbildning och erfarenhet

- Minst gymnasieutbildning, gärna inom naturvetenskap eller vård. Vi ser gärna att du har universitets- eller högskoleutbildning som biomedicinsk analytiker eller motsvarande.
- God datorvana
- Goda språkkunskaper i svenska och engelska


Erfarenhet av arbete inom kliniska prövningar och inom regelverket GCP är meriterande för rollen. Därtill ser vi även det som fördelaktigt med kunskap och intresse inom programmering.

Övrig information

För mer information om tjänsten, kontakta Anna Ringheim Cadete, Corelab Manager, på 073-233 00 03 alt. [email protected]

Om du vill veta mer om Antaros Medical och vår verksamhet, kika in på vår hemsida för att lära dig mer: www.antarosmedical.com (http://www.antarosmedical.com)

Skicka din ansökan (ett kort personligt brev och ditt CV) senast den 31st October 2021 . Intervjuer kommer att ske löpande. Vi tar endast emot ansökningar via vårt rekryteringssystem Teamtailor. Samtal från externa rekryteringsföretag och säljare undanbedes. Visa mindre

Clinical Project Manager to Antaros Medical

Ansök    Sep 28    Antaros Medical AB    Utvecklingschef
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imagin... Visa mer
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in Swedish and English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than 31st October, 2021.

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected]

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Clinical Project Manager to Antaros Medical

Ansök    Sep 3    Antaros Medical AB    Utvecklingschef
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imagin... Visa mer
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in Swedish and English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than 30th September, 2021.

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected]

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Software Developer to Antaros Medical

Ansök    Sep 27    Antaros Medical AB    Utvecklingschef
Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future? Are you a person who enjoys a dynamic environment and to be part of a growing team with software developers and specialists? If it ticks your boxes, you should continue reading. At Antaros Medical, we value competence and de... Visa mer
Does software development of image processing and analysis tools catch your eye? How about working in an innovative company within the global Life Science sector where your work contributes to improving drug development of the future? Are you a person who enjoys a dynamic environment and to be part of a growing team with software developers and specialists? If it ticks your boxes, you should continue reading.

At Antaros Medical, we value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 80 employees working at our offices in Sweden in Mölndal and Uppsala, as well as in the US, and we are continuously growing. As a part of our growth journey, we are looking for our next experienced Software Developer for implementation and validation of software used in clinical trials, to join our Uppsala office.

As a Software Developer, you will join a growing team of software developers and specialists in image processing and image analysis. You will further be part of cross-functional project teams in clinical trials, coordinating software development solutions in the project. This includes working with many different roles in the company such as project management and internal end-users of software. You will be responsible for software development of tools for managing and analysing medical images acquired in clinical trials, consisting of MR and PET images.

You will further support with verification and validation of developed as well as acquired software, including requirement management and test protocol creation.

In addition, your work role will include support in method development and medical image processing.

Your main responsibilities will be:

- Development of software tools for medical image management, processing, and analysis.
- Validation of software for analysis of medical imaging data.
- Maintenance and internal support for developed software.


Additional responsibilities could include:

- System owner of applicable computerised systems.

Who are we looking for?

We believe that you have been working with professional software development, preferably with medical images, and including verification and validation, for at least 4 years. You are keen on working both independently as well as in teams with software development of image management and image processing systems.

As a person, you have a logic mindset and analytic ability to solve and conclude issues of different character. You are creative by thinking outside the box and approaching a problem from different angles. We further believe that you have demonstrated collaborative and communicative skills to engage with colleagues and clients, including colleagues with other backgrounds than software development. You have the flexibility and ability to meet deadlines while being thorough and delivering high quality work in a dynamic environment.

Requirements:

- 4+ years’ experience of professional software development, including verification and validation
- B.Sc. degree in relevant field
- Proficiency in Python


It is meritorious if you have previous work experience of GCP/GAMP, as well as software development within a regulated industry, such as medical device development or clinical trials, including experience from medical images of MR and PET. It is further perceived as beneficial if you have studied computer science, engineering physics, applied systems science, and/or software development. Longer experience with software development is meriting.

In addition, we perceive professional knowledge of Matlab, C++, AWS, and requirement management to be of advantage in the work role.

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter (in English) and your CV included, no later than 31st October 2021.

For more information about the position, please contact Carl Sjöberg, Director Image Processing and Software Development, [email protected] +46 73 050 04 69

The recruitment is for a permanent employment.

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialised in cardiorenal & metabolic diseases and oncology.

We combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. Visa mindre

Mandarin speaking Clinical Project Manager to Antaros Medical

Ansök    Aug 19    Antaros Medical AB    Utvecklingschef
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imagin... Visa mer
Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in Swedish and English
- Excellent written and verbal communication skills in Mandarin


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than 19th September, 2021.

For more information about the position, please contact Emilia Larsson, +46 73-728 93 43, or [email protected]

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Team Lead Hardware Development

Ansök    Jun 28    Cytiva Sweden AB    Utvecklingschef
Hjälp oss att förbättra tillgången till livsavgörande behandlingar som kan förändra människors hälsa Vi är Cytiva, en global leverantör av teknologier och tjänster som främjar och påskyndar utvecklingen och tillverkningen av terapier. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020. Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vaccin... Visa mer
Hjälp oss att förbättra tillgången till livsavgörande behandlingar som kan förändra människors hälsa
Vi är Cytiva, en global leverantör av teknologier och tjänster som främjar och påskyndar utvecklingen och tillverkningen av terapier. Som tidigare del av GE Healthcare har vi ett rikt arv av värdefull erfarenhet och en nystart sedan 2020.
Våra kunder bedriver livsavgörande forskning och produktion, alltifrån biologisk forskning till utveckling av nya vacciner, läkemedel, cell- och genterapier. Vårt uppdrag är att leverera verktygen och tjänsterna som de behöver, allt för att kunna leverera snabbare och säkrare vård till patienter.
Vi söker en team leader till ett av våra hårdvaruteam. Du kommer leda ett team med ingenjörer inom elektronik, mekanik, embedded, optik och testning. Tillsammans utvecklar ni nästa generations system för läkemedel och vaccinframställning. Är du intresserad av att leda andra och samtidigt hjälpa till att designa och förbättra produkter? Då vill vi höra ifrån dig.
Arbetsuppgifter
Leda och koordinera arbetsuppgifter i ett team med ca 10 ingenjörer inom mekanik, elektronik, optik, embedded och testning.
Säkerställa att designen på våra produkter möter våra projektmål för en effektiv överföring till produktion och service.
Stötta teamet i design av våra system. Bidra med kunskap gällande design, lösningar, komponenter, verktyg, metoder och utredningar..
Designa produkter som innehåller robotar, pumpar, ventiler, detektorer och mycket mer.
Utveckla våra agila arbetssätt tillsammans med våra team och andra team leads

Vem är du?
Minst högskoleingenjör med 5 års relevant arbetslivserfarenhet
Stort eget driv och tekniskt intresse med vilja att utvecklas
Erfarenhet av att arbeta med design från utvecklingsfas till produktion, gärna i en agil miljö
Flytande i svenska och engelska, såväl tal som skrift.



Vilka är vi?
Oavsett din roll, ger vi dig ett syfte och en utmaning varje arbetsdag. Om du drivs av att göra världen till en bättre plats genom vetenskap och medicin, kommer du att känna dig hemma här. Är du flexibel, nyfiken och envis är du rätt person. Trivs du dessutom i en global kultur, kan detta vara platsen för din fortsatta karriär.
Urval och intervjuer sker löpande och sista ansökningsdag är 8e Augusti. För frågor kontakta gärna Thomas Arctaedius, [email protected]
Vill du veta mer? Spana in vår Careers webbsida (https://jobs.danaher.com/global/en/cytiva) , Instagram-kanal (https://www.instagram.com/cytiva/) och LinkedIn-sida (https://www.linkedin.com/company/cytiva/) !
Cytiva är en global ledare inom biovetenskap med nästan 7 000 anställda i 40 länder som är hängivna vårt uppdrag att främja och påskynda behandlingar. Som en pålitlig partner till kunder världen över bidrar Cytiva till ett effektivt arbetsflöde till forskning och utveckling, säkerställer tillverkning och leverans av omvälvande mediciner till patienter.
Cytiva är en del av Danaher-familjen, en global nyskapare inom vetenskap och teknologi som är hängiven att hjälpa kunder att lösa komplexa utmaningar samt förbättra livskvaliteten välden över. Visa mindre

Quality Assurance Director

About the role Bio-Works is looking to strengthen its Quality Assurance team with a director-level role tasked with defining and promoting a quality mindset across the entire company. The QA Director is responsible for managing all QA functions, working with cross-departmental leadership to deliver high-quality products on schedule. Responsibilities - Assures quality products and processes by establishing and enforcing quality standards and testing mate... Visa mer
About the role

Bio-Works is looking to strengthen its Quality Assurance team with a director-level role tasked with defining and promoting a quality mindset across the entire company. The QA Director is responsible for managing all QA functions, working with cross-departmental leadership to deliver high-quality products on schedule.

Responsibilities

- Assures quality products and processes by establishing and enforcing quality standards and testing materials and products per ISO 9001:2015.
- Develop the QA function according to Bio-Works' strategic plan
- Act independently of Bio-Works management in handling QMS resources and activities
- Create product quality documentation system by writing and updating quality assurance procedures.
- Maintain product quality by enforcing quality assurance policies and procedures and government requirements.
- Collaborate with other members of management to develop new product and engineering designs and manufacturing and training methods.
- Prepare product and process quality reports by collecting, analyzing, and summarizing information and trends.
- Complete quality assurance operational requirements by scheduling and assigning employees and following up on work results.
- Develop a quality assurance staff by recruiting, selecting, orienting, and training employees.
- Manage quality assurance staff job results by coaching, counseling, and disciplining employees.
- Ensure quality by planning, monitoring, and appraising job results.
- Maintain professional and technical knowledge by attending educational workshops, reviewing professional publications, establishing personal networks, and participating in professional societies.
- Achieve financial objectives by preparing the quality assurance budget, scheduling expenditures, analyzing variances, and initiating corrective actions.
- Contribute to team effort by accomplishing related results as needed.


Requirements (skills)

- BA or BS in appropriate discipline
- Five to 10 years’ experience as QA manager or director in ISO 9001:2015 company
- Working knowledge of quality system requirements
- Experience with MS Word, Excel, Project Management and Analytics software
- Strong communication, negotiation, and management skills.
- Business fluency in English and Swedish are required.
- Experience with LEAN / KANBAN / Six Sigma is a plus.


Requirements (personality)

- Strong leadership skills both in terms of self-leadership and leading teams
- A proactive risk-based attitude focused on identifying problems and solutions.
- A collaborative mindset
- A precise and analytic mindset to identify and focus on issues and risks.




Do you have a question?

For any questions, you are warmly welcomed to contact Jonathan Royce at [email protected] Visa mindre

Quality Assurance Director

About the role Bio-Works is looking to strengthen its Quality Assurance team with a director-level role tasked with defining and promoting a quality mindset across the entire company. The QA Director is responsible for managing all QA functions, working with cross-departmental leadership to deliver high-quality products on schedule. Since we are still a relatively young company, many things are yet to be set, invented, discovered, fixed… We think this i... Visa mer
About the role

Bio-Works is looking to strengthen its Quality Assurance team with a director-level role tasked with defining and promoting a quality mindset across the entire company. The QA Director is responsible for managing all QA functions, working with cross-departmental leadership to deliver high-quality products on schedule.

Since we are still a relatively young company, many things are yet to be set, invented, discovered, fixed…

We think this is something that triggers you.

Responsibilities

- Assures quality products and processes by establishing and enforcing quality standards and testing materials and products per ISO 9001:2015.
- Develop the QA function according to Bio-Works' strategic plan
- Act independently of Bio-Works management in handling QMS resources and activities
- Create product quality documentation system by writing and updating quality assurance procedures.
- Maintain product quality by enforcing quality assurance policies and procedures and government requirements.
- Collaborate with other members of management to develop new product and engineering designs and manufacturing and training methods.
- Prepare product and process quality reports by collecting, analyzing, and summarizing information and trends.
- Complete quality assurance operational requirements by scheduling and assigning employees and following up on work results.
- Develop a quality assurance staff by recruiting, selecting, orienting, and training employees.
- Manage quality assurance staff job results by coaching, counseling, and disciplining employees.
- Ensure quality by planning, monitoring, and appraising job results.
- Maintain professional and technical knowledge by attending educational workshops, reviewing professional publications, establishing personal networks, and participating in professional societies.
- Achieve financial objectives by preparing the quality assurance budget, scheduling expenditures, analyzing variances, and initiating corrective actions.
- Contribute to team effort by accomplishing related results as needed.


Requirements (skills)

- BA or BS in appropriate discipline
- Experience as QA manager in an ISO 9001:2015 company
- Working knowledge of quality system requirements
- Experience with MS Word, Excel, Project Management and Analytics software
- Business fluency in English and Swedish are required
- Strong communication and negotiation skills
- Experience with LEAN / KANBAN / Six Sigma is a plus


Requirements (personality)

- Strong leadership skills both in terms of self-leadership and leading teams
- A proactive risk-based attitude focused on identifying problems and solutions
- A collaborative mindset
- A precise and analytic mindset to identify and focus on issues and risks



Do you have a question?

For any questions, you are warmly welcomed to contact Jonathan Royce at [email protected] Visa mindre

Senior Regulatory Affairs Manager to Galderma

Ansök    Mar 16    Q-Med AB    Utvecklingschef
About Galderma Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically prove... Visa mer
About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com.

Job description / Arbetsbeskrivning

The Regulatory Affairs Department at Galderma Uppsala is responsible for all Regulatory aspects of Galderma's aesthetic business at Global level. This includes new product registrations, line extensions and Life Cycle Management of the portfolio of products for both Pharmaceuticals and Medical Device. We manage a broad portfolio of products across almost 90 markets and are expanding our scope with several new innovation projects in our pipeline.

We are now expanding our Medical Device Regulatory Team in Uppsala and looking for a Senior Regulatory Affairs Manager to take on a roll within the team.

Job responsibilities / Ditt uppdrag

About the role
As Senior Regulatory Affairs Manager you will represent Regulatory Affairs as Regulatory Lead in key development and life cycle management projects. You will be responsible for co-ordination and dossier compilation. The role also includes managing Life Cycle Management activities including variations, renewals, labelling changes etc.

Your responsibilities would include:

* Act as Global Regulatory lead within multi-functional project teams, provide support and influence decision-making in order to enable project delivery within defined targets.

* Analyze regulatory requirements and develop regulatory strategies world-wide, including active communication with local Regulatory Authorities and Galderma affiliates.

* Deliver high quality regulatory documentation for all activities either Development projects or Life Cycle Management Projects.

* Represent Regulatory Affairs in internal and external audits.
* Geographical Expansion of the portfolio

* License maintenance
* Surveillance of regulatory requirements - at Global level

Minimum requirements/ Är du den vi söker?

About you

* You hold a university degree in a life science area such as Pharmaceutical Science or similar.
* You also have several years' experience of Regulatory Affairs within the Pharmaceutical or Medical Device industry, or from an Authority (Health authority, Notified Body or similar) perspective.
* You have experience of compiling and reviewing documents/reports according to Global regulatory guidelines.
* You are open-minded and willing to adapt to changes and enjoy working with others in a collaborative way, also across several cultures
* You are self-driven, flexible, methodical, with the ability to structure work and manage multiple requests while maintaining timelines
* You possess good communication skills and fluency in Swedish and English, both verbal and written. Strong writing, reading and reviewing skills are necessary.



Other important information/ Frågor och ansökan

What we offer in return
As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 450 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.



Your application
We welcome your application (CV and letter) via our company website

https://www.galderma.com/job-search or by clicking "Apply Now" below.

Apply as soon as possible though no later than 13th April. The selection process is ongoing.



Should you have questions about this opportunity you are welcome to contact

Sinéad Breen, Global Head of Regulatory Affairs at +46 768981230 Visa mindre

Head of R&D Project Management

Ansök    Mar 11    Q-Med AB    Utvecklingschef
About Galderma Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically prove... Visa mer
About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com.

Job description / Arbetsbeskrivning

The role as Head of R&D Project Management is a unique opportunity to join Galderma's innovation engine - Global R&D is committed to accelerate product development and further grow the business. The position is an integral part in Galderma's growth journey to become the world's leading dermatology company, this with existing and new products in both medical device and drug manufacturing.

The responsibility spans from managing the R&D project portfolio to leading and managing the team - fostering a culture balancing a winning mindset with strong core values. As a key leader in Global R&D, the incumbent will be interacting with top management and multiple stakeholders across Galderma. In order to achieve this, the Head of R&D Project management will work through the team of project managers by setting targets and strategies as well as by mentoring and coaching the team. The Head of R&D Project Management will report to Head of Portfolio, Project Management & Early Development and is based at Galderma Uppsala site.

Job responsibilities / Ditt uppdrag

* Lead and develop the team of high performing R&D Project Managers; set plans and objectives to monitor progress and overall ensure the output: reaching targets and objectives which support the short-, mid- and long-term strategy for R&D.
* Ensure adequate information is provided to the portfolio management team on the status, budget, and forecast of portfolio projects.
* Provide leadership in the harmonization and implementation of a consistent development operating model across Rx and Ax, working closely with key stakeholders (e.g. R&D, GBUs, Operations).
* Be an active member of the Portfolio, Project Management & Early Development Leadership Team and the Pipeline Committee, building strong relationships across geographies, to ensure partnership and collaboration.
* Continuously develop the R&D Project Management function to ensure the knowledge, the tools and means to effectively meet R&D objectives. Lead and decide on the development and implementation of methods/processes, working procedures and documentation needed to fulfil the areas of appointed responsibilities.
* Manage all people processes for the Project Management team such as performance, talent management and recruitment

Minimum requirements/ Är du den vi söker?

* Minimum of 5 years of experience from leading a project management team in an international setting- including empowerment of others and team building
* Extensive experience (minimum 10 years) of working in projects, towards deadlines and leading development/change activities
* Several working years in R&D within the pharmaceutical, medical devices and/or biotechnology area
* Experience in driving product development projects in collaboration with external parties
* Fluent in both written and spoken English

Other important information/ Frågor och ansökan

In this recruitment we are partnering with the executive search firm Ahrle Laurell & Partners. Please send your CV and cover letter as soon as possible, but no later than March 25th 2021, to [email protected] Visa mindre

Manager Technical Development and Maintenance I&D

Ansök    Mar 9    Fresenius Kabi AB    Utvecklingschef
Fresenius Kabi har en global forsknings- och utvecklingsorganisation som ansvarar för produktutveckling och strategisk marknadsföring inom företagets olika verksamhetsområden. I Sverige finns enheten för Forskning och Utveckling inom Parenteral nutrition, (PN), som är lokaliserad i anslutning till produktionsanläggningen i Uppsala. Verksamheten omfattar farmaceutisk och analytisk utveckling och dokumentation av nya PN produkter, och arbetet bedrivs i proje... Visa mer
Fresenius Kabi har en global forsknings- och utvecklingsorganisation som ansvarar för produktutveckling och strategisk marknadsföring inom företagets olika verksamhetsområden. I Sverige finns enheten för Forskning och Utveckling inom Parenteral nutrition, (PN), som är lokaliserad i anslutning till produktionsanläggningen i Uppsala. Verksamheten omfattar farmaceutisk och analytisk utveckling och dokumentation av nya PN produkter, och arbetet bedrivs i projektform tillsammans med strategisk marknad, preklinisk och klinisk utveckling, som är lokaliserad till Tyskland, och registreringsavdelningen, som också finns i Uppsala. En mycket viktig del är samverkan med produktionsenheterna, såväl i Uppsala som på andra platser, för uppskalning och tillverkning under utvecklingsprocessens gång.

Fresenius Kabi i Uppsala söker en Manager Technical Development & Maintenance för att leda en nyligen skapad supportgrupp med ansvarsområdet teknisk utveckling och underhåll inom avdelningen Innovation & Development (I&D) Center Sweden. I&D Center Sweden utvecklar nya resp förbättrar befintliga produkter inom parenteral nutrition. Avdelningen består av fyra grupper som sammanlagt omfattar ett trettiotal medarbetare. Utvecklingsarbete bedrivs i projektform samt följer GMP regler och andra myndighetskrav. Som Manager Technical Development & Maintenance leder du en grupp om tre medarbetare som ansvarar för förebyggande underhåll av befintlig utrustning, inköp av ny utrustning, underhåll av lokaler och hantering av stabilitetsstudier. Även dataintegritetsfunktionen ligger inom gruppens ansvar. Därutöver arbetar gruppen med teknisk utvärdering av nya tekniker (tillverkning/mät/analys). Du rapporterar till Vice President I&DC; Sweden och ingår i avdelningens ledningsgrupp.

 

Arbetsuppgifter inom tjänsten:

Leda gruppen Technical Development & Maintenance och planlägga gruppens arbete.
Sätta mål för gruppen och dess medarbetare utifrån avdelningens övergripande mål och följa upp på gruppens KPI:er.
Inspirera, motivera och kompetensutveckla gruppens medarbetare.
Planera och följa upp budgeten för gruppens ansvarsområde samt för avdelningens capex projekt.
Deltaga i avdelningens ledningsgrupp.
Ansvara för att arbetsmiljölagar och GMP regler följs.
Planera, utföra och avrapportera underhållsaktiviteter för avdelningens utrustning, instrument och datoriserade system.
Underhålla avdelningens instrumentregister.
Delta i kvalitetsarbetet inom funktionen.
Upprätta och granska styrande och redovisande kvalitetsdokument inom ansvarsområdet.
Genomföra utvärdering och inköp av utrustning.
Initiera och deltaga i avdelningens förbättringsarbete.
 

Kvalifikationer:

Vi söker dig med akademisk utbildning inom kemi/kemiteknik, farmaci eller motsvarande. Du har minst fem års erfarenhet från läkemedelsindustrin eller annan relevant industri och är förtrogen med GMP-regelverk. Vi ser gärna att du har en viss ledarskapserfarenhet, t ex som linjechef eller projektledare. Kunskap inom dataintegritet/datoriserade system är en merit. Du måste ha goda kunskaper i både svenska och engelska i både tal och skrift.

 

Personliga egenskaper och kompetenser som vi värderar är:

Mycket god kommunikations- och samarbetsförmåga, då tjänsten kräver samverkan och samarbeten med andra grupper både i Sverige men även internationellt.
God planerings- och problemlösningsförmåga samt stort intresse av tekniska frågeställningar.
Du är kvalitetsmedveten, resultatorienterad, sätter ambitiösa mål och levererar i tid.
Som chef är du en förebild och motiverar dina medarbetare. Du är entusiastisk och positiv även i tuffa situationer.
Du söker nya perspektiv och idéer för att stimulera innovation och förändring.
Prioriteringsförmåga.
 

Uppdragsgivare: Fresenius Kabi

Ort: Uppsala

Omfattning: Heltid tillsvidare. Anställningen inleds med 6 månaders tidsbegränsad visstidsanställning (motsvarande provanställning).

Sista ansökningsdag: 31 mars 2021. OBS, utvärdering och intervjuer sker löpande. Tjänsten kan därför bli tillsatt innan sista ansökningsdatum.

 

För information: För frågor, kontakta ansvarig chef Britta Siekmann 018-644 389. För oss är det viktigt att all kompetens på arbetsmarknaden tillvaratas. Vi välkomnar alla sökande och eftersträvar mångfald. Fackliga kontaktpersoner är Frank Glackin för Unionen, 018-644 773 och Linda Holm för SACO, 018-644 195. Visa mindre

Project Manager to Galderma

Ansök    Nov 30    Q-Med AB    Utvecklingschef
About Galderma Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically prove... Visa mer
About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com.

Job Description

As a Project Manager, will you provide day-to-day project management to global drug/medical device development project teams in the Aesthetics Global Business Unit. In close collaboration with other functions within the company, you will drive the Aesthetics innovation pipeline progression to ensure timely supply of quality products to our customers and contribute to Galderma's short- and long-term growth.

Job Responsibilities

As Project Manager, you will:

* Manage global cross-functional teams of professionals responsible for product development from early stage until launch.
* Be accountable for project objectives, deliverables, timeline and budget.
* Manage project decision making.
* Be responsible for developing and communicating strategies, goals and long-term vision for projects.
* Implement and organize actions to improve team motivation and shared understanding.
* Ensure and facilitate cross-functional collaboration.
* Assess project risks with the project team, propose and follow-up mitigation and contingency plans.
* Ensure appropriate reporting of project progression inside and outside the team.
* Issue the project core documentation.

Minimum Requirements

We believe that you have a university degree within science, engineering or business. You have solid experience as project manager, with specific experience from the pharmaceutical industry including clinical development. You are used to working in an international environment.



We think that you have the following skills and competences:

* Excellent skills in project management tools and practices.
* Excellent communication skills, both oral and written communication.
* Good team leadership skills.
* Good financial knowledge.
* An analytical and strategic mindset.
* Experience in change management.

We also believe that you are courageous, ambitious and goal-oriented. You know how to influence others and you have integrity and an open mind.



What we offer in return

As Galderma's Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole chain from product development to production. Here our 450 employees work on our world leading brands such as Restylane®, Azzalure® and Sculptra®.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10-minute bike ride from Uppsala Central Station.



Your application

We welcome your application (CV and letter) via our company website https://www.galderma.com/job-search. Apply as soon as possible though no later than December 14. The selection process is ongoing.

Should you have questions about this opportunity you are welcome to contact recruiting manager Malin Johansson on phone number 018-4891498. Visa mindre

Konstruktionschef till Rolba

Om företaget Rolba Svenska AB i Hedesunda grundades 1962, verksamheten omfattar alla steg från idé till leverans av färdig produkt. Företaget omsätter ca: 190 mkr och är idag 55st anställda. Vår personal kännetecknas av bred kompetens med ett personligt engagemang. Våra marknadsandelar ökar stadigt i Sverige, Finland, Norge, Danmark samt England och vi är en ledande tillverkare av högkvalitativ utrustning för slamsugning, högtrycksspolning monterade på la... Visa mer
Om företaget

Rolba Svenska AB i Hedesunda grundades 1962, verksamheten omfattar alla steg från idé till leverans av färdig produkt. Företaget omsätter ca: 190 mkr och är idag 55st anställda. Vår personal kännetecknas av bred kompetens med ett personligt engagemang. Våra marknadsandelar ökar stadigt i Sverige, Finland, Norge, Danmark samt England och vi är en ledande tillverkare av högkvalitativ utrustning för slamsugning, högtrycksspolning monterade på lastbilschassier. Vår kundkrets finns inom företag och kommuner. Läs mer på www.rolba.se

Dina arbetsuppgifter

Vi söker en konstruktionschef

Rolba har en stor produktionsanläggning i Hedesunda som idag är hjärtat av verksamheten med ett huvudkontor där ledning, produktutveckling och produktion finns under samma tak. Rolba ansvarar för hela operativa Supply Chain, från R&D till After Sales. Rolba präglas av ett intensivt och mångsidigt förbättringsarbete för att säkra företagets strävan till fortsatt tillväxt och att etablera sig som en marknadsledande koncern. Kvalitet, Service och Effektivitet är några av våra viktigaste framgångsfaktorer.

Konstruktionsavdelningen utgör en viktig komponent i vår framgång. Avdelningen ansvarar för att koncernen har en konkurrenskraftig produktportfölj samt driver ett antal stora och små projekt på en relativt högteknisk nivå. Vårt team arbetar ständigt för att säkerställa att tillverkningsprocessen når de kort- och långsiktiga mål vad det gäller kostnadseffektivitet, produktivitet, leveransprecision och kvalitet.

Arbetsuppgifter

Att arbeta hos oss innebär att arbeta i ett högt tempo i en kreativ och spännande miljö, ofta med flera parallella uppdrag. Tillsammans med duktiga medarbetare kommer du att direkt påverka våra produkter och företagets förmåga att nå sina mål. Du kommer till en flexibel organisation där du har stora möjligheter att påverka ditt arbete. Som konstruktionschef i på Rolba ingår du i företagets ledningsgrupp.

Om du dessutom vill få utlopp för din kreativitet och ”triggas” av att se ditt avdelningsarbete utvecklas från tanke till färdig produkt kommer du att trivas hos oss. Utveckling, Modularisering, Design samt löpande ritningsarbete är vanliga uppgifter på avdelningen där du blir en viktig del i att leda och fördela arbetet på bästa sätt för att nå uppsatta mål för avdelningen och företaget. I tjänsten ingår också fullt personalansvar för din avdelning bestående av 5 personer med kompetens inom hydraulik, el, 3D CAD, mekanisk konstruktion samt högtycksspolning och vakuumteknik.

Din profil

Vi söker dig som har ett genuint intresse av ledarskap!

För att lyckas i din roll är du en person som har viljan att ta ett stort ansvar. Du trivs med att leda och driva ditt team mot uppsatta mål och har stort fokus på att uppnå resultat. Att samarbeta med olika avdelningar är en självklarhet för dig och du finner stor glädje i att engagera och entusiasmera dina kollegor.

Din kompetens är också viktigt för oss.
För att bli framgångsrik i din roll som konstruktionschef på Rolba ser vi att du har erfarenhet eller utbildning inom arbetsledning, personalansvar och projektledning samt besitter en god teknisk förståelse. Vi ser det som meriterande om du har erfarenhet av att jobba nära kunder, besitter ett genuint teknikintresse och har praktiskt erfarenhet av tillverkning. Har du dessutom erfarenhet från fordonsindustrin, design och konstruktion, är utbildad Högskole- eller civilingenjör inom maskinkonstruktion eller motsvarande är det mycket meriterande.

Ansökan

I den här rekryteringen samarbetar vi med Clockwork Rekrytering & bemanning. För mer information om tjänsten är du varmt välkommen att kontakta rekryteringskonsult Poria Shademani på tel. 0733512720 [email protected] Vi arbetar med rekryteringsprocessen löpande, så ansök så snart som möjligt via www.clockworkpersonal.se Visa mindre

SHE Manager to Galderma

Ansök    Dec 10    Q-Med AB    Utvecklingschef
About Galderma Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically prove... Visa mer
About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com.

Job Description

Would you like to manage the SHE development in a large, successful medical device company with focus on Change Management? Galderma in Uppsala is working in a fast-growing business where we are currently investing in a wide range of exciting projects that will shape our future.

Job Responsibilities

As SHE Manager at Galderma Aesthetics in Uppsala, you have the overall responsibility for developing and maintaining the Safety, Health and Environment (SHE) Management System at the Site. You will lead the work to maintain certifications according to ISO 14001 and ISO 45001 as well as drive our long-term commitment to environmental sustainability and wellbeing of our employees.

Your role will include:

* Develop and maintain an appropriate and effective SHE Management system for the site, including established objectives and processes necessary to deliver results in accordance with legal requirements and the company's Safety, Health and Environment policies.
* SHE development within the site of our current technical platform as well as enabling future needs of new facilities, utilities, manufacturing processes and new product technologies.

* Inspire employees at all levels through training, dialogue and communication to engage proactively in SHE initiatives in the workplace and beyond, including awareness, education and good practice sharing.

* Implement assessment of environmental impacts in the formulation, packaging design, manufacturing and distribution of new and reformulated products

* Track and reduce our direct and indirect greenhouse gas emissions, water use and waste, thereby contributing to a sustainable future.

* Manage the SHE team consisting of 3 senior SHE experts including budget and personnel responsibility in line with Company policies and processes as well as defined key activities to drive the SHE related topics in an adequate way.

Minimum Requirements

* You have a University-degree, minimum at Bachelor level or an equivalent education in engineering, science, or business
* You have min 10 years of experience gained in a fast-paced manufacturing environment.
* In addition, you bring 5 years' experience from a manager position
* You possess strong communication skills
* You are used to work in forms of projects and have the ability to prioritize and manage multiple tasks and meeting all agreed deadlines
* You are very results oriented, possess a business acumen, and have a strong sense of urgency in meeting customer needs
* You are fluent in Swedish and have a good command of English
* You have good working experience from ISO 14001 and ISO 45001

As SHE Manager your leadership skills are in focus. You are a confident manager with diplomatic skills and courage. You display both integrity and understanding for the overall organizational needs. As a leader, you have the ability to listen, coach, delegate, make decisions, acting in an accountable way and support your colleagues. You are strong in Change Management.

Other Important Information

We welcome your application (CV and letter) via this career site or via our company website https://www.galderma.com/job-search

. You will be able to create a personal account and upload your application documents. Apply as soon as possible though no later than Jan 7th.

For further questions, please contact our HRBP Celine Bales Visa mindre

Teknisk Chef (CTO)

Ansök    Jun 4    Airwatergreen AB    Utvecklingschef
CTO till Sveriges torraste bolag Om rollen Du kommer att få vara med och sätta en ny standard för avfuktning i världen där vi hjälper våra kunder till ett bättre inneklimat och sänker deras energiförbrukning. Med ett fokus på hållbarhet och långsiktig lönsamhet. Som CTO kommer du att ansvara för utvecklingen av våra nya produkter samt vidareutveckling av våra befintliga. Alla baserade på patenterad och unik teknologi som innebär ett skifte i denna marknad.... Visa mer
CTO till Sveriges torraste bolag
Om rollen
Du kommer att få vara med och sätta en ny standard för avfuktning i världen där vi hjälper våra kunder till ett bättre inneklimat och sänker deras energiförbrukning. Med ett fokus på hållbarhet och långsiktig lönsamhet.
Som CTO kommer du att ansvara för utvecklingen av våra nya produkter samt vidareutveckling av våra befintliga. Alla baserade på patenterad och unik teknologi som innebär ett skifte i denna marknad. Du kommer att vara medlem i företagets ledningsgrupp och ansvara för hela utvecklingsprocessen i nära samarbete med övriga medarbetare, partners, leverantörer och i direkt kontakt med våra kunder.
Efter introduktion på huvudkontoret i Uppsala tror vi att du är självgående, kan uppvisa ett stort driv och hämta motivation från att vi tillsammans kan förändra vardagen för våra kunder genom våra produkter.


Om bolaget
Airwatergreen AB är ett svenskt luftbehandlingsbolag som erbjuder energieffektiv avfuktning i alla klimat. Vi utvecklar och tillverkar produkter som avlägsnar fukt och lukt på ett effektivt sätt vilket förlänger livslängden på byggnader, varor och utrustning, samt skapar en hälsosammare arbetsplatsmiljö att vistas i. Vi har idag nära 600 installationer i 8 länder.
Produkterna bygger på våra patenterade teknologier som ger en rad unika fördelar. Fördelar som halverad energiförbrukning, enkelhet att installera och samma effektivitet vid alla temperaturer. Vi har nu startat arbetet med att ta fram nästa generation av produkter som kommer att ytterligare bredda och stärka vårt erbjudande.
Vi har kontor i Uppsala och Malmö samt partners i ett antal Europeiska länder.


Din kompetens och profil
Du har en bakgrund inom att leda utveckling och framtagning av tekniska produkter som består av både hårdvara och mjukvara. Har du dessutom arbetat med liknande produkter eller hos någon av de större teknikkonsulterna, så har du en riktigt stark bakgrund. Ett befintligt nätverk inom exempelvis VA-branschen eller ventilationsbranschen är en tillgång.
Dina framtida kollegor är alla målmedvetna och ambitiösa så att du är energisk och motiverad ser vi som självklart.
Vi sätter stort fokus på hur du är som person och vad du vill uppnå med oss då vi jobbar tillsammans mot tuffa mål. Du bör ha en förmåga att övertyga och en vana av att kunna förklara komplexa saker på ett lättförståeligt sätt. En akademisk examen inom relevant teknikområde behövs kombinerat med en vilja att kavla upp ärmarna och få jobbet gjort.
Några ytterligare krav:
Erfarenhet och kunskap av Teknisk utveckling - produktframtagning
Vana att arbeta med Strategi – Marknadskrav – Utveckling
Flytande svenska och engelska i både tal och skrift



Ansökan
Jobbet blir ditt så fort som möjligt och intervjuer sker löpande på vårt Uppsalakontor. Du söker tjänsten via denna annons och glöm inte att bifoga CV samt en personlig presentation om vem du är och varför du är lämpad för rollen.
Har du frågor eller funderingar kring tjänsten är du välkommen att kontakta Bo Tiderman vår VD via e-mail [email protected]


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PMO & Development Manager

Ansök    Jan 23    Svensk Dos AB    Utvecklingschef
Svensk Dos tillverkar och levererar dosdispenserade läkemedel och har kunder från norr till söder. Svensk Dos grundades 2013 av fyra apotekare från Uppsala, och är sedan 2016 ett helägt dotterbolag till finska Oriola Corporation som är noterat på Helsingfors Fondbörs. I koncernen ingår även läkemedelsdistributören Oriola AB, apotekskedjan Kronans Apotek och supportföretaget ICT Health Support. Vi finns i Fyrislund, Uppsala och har idag drygt 200 anställda.... Visa mer
Svensk Dos tillverkar och levererar dosdispenserade läkemedel och har kunder från norr till söder. Svensk Dos grundades 2013 av fyra apotekare från Uppsala, och är sedan 2016 ett helägt dotterbolag till finska Oriola Corporation som är noterat på Helsingfors Fondbörs. I koncernen ingår även läkemedelsdistributören Oriola AB, apotekskedjan Kronans Apotek och supportföretaget ICT Health Support. Vi finns i Fyrislund, Uppsala och har idag drygt 200 anställda. I dagsläget levererar Svensk Dos läkemedel till ca 95 000 patienter i Region Skåne, Norra sjukvårdsregionen, Region Stockholm, Region Gotland samt till patienter inom Kriminalvården. Vi har kollektivavtal med Unionen och är anslutna till Tjänstemannaavtal apotek. Utöver en trevlig arbetsplats har vi bl.a. ett av branschens bästa friskvårdsbidrag.

 Om arbetet

Svensk Dos består av farmaci, produktion, logistik, kundtjänst samt stödfunktionerna kvalitet, sortiment och teknik & underhåll. Nu söker vi en PMO & Development Manager som ska säkerställa att företagets standarder är tydligt definierade och följs genom hela projektprocessen. Tjänsten innebär även ansvaret att coacha och stödja utvecklingen av Leanarbetet inom företaget. Rollen ingår i koncernens Operational Excellence-nätverk där kollegor från både Sverige och Finland ingår.PMO & Development Manager ingår i ledningsgruppen och rapporterar till platschefen.

 Ditt uppdrag

I rollen som PMO & Development Manager har du till uppgift att initiera och leda utvecklingsaktiviteter och projekt inom företaget, allt från metoder, processer och standarder, och säkerställa implementeringen av de gemensamma processerna. Du följer upp företagets mål och analyserar avvikelser, definierar och initierar förebyggande åtgärder. Rollen coachar och stödjer utvecklingen av det fortsatta Leanarbetet i nära samarbete med övriga chefer och medarbetare. Du administrerar och upprätthåller företagets ledningssystem tillsammans med företagets kvalitetsavdelning. Du ansvarar att följa rutiner baserade på föreskrifter och GDP/GMP inom det egna ansvarsområdet. 

Din profil

Vi söker dig som är högskole- eller universitetsutbildad inom projektledning, teknik, logistik eller supply chain med 1–2 års erfarenhet av ledarskap inom tillverkning eller liknande verksamhet. Du är väl förtrogen med projektledning, ledningssystem och har god datakunskap motsvarande Officepaketet. Du kommunicerar både på svenska och engelska och tycker om att samarbeta med både interna kollegor, olika avdelningar inom koncernen och kunder/leverantörer.

För denna tjänst lägger vi även stor vikt vid dina personliga egenskaper. Du är analytisk och har en klar förmåga att samarbeta, entusiasmera och coacha andra. Du är självständig och går från ord till handling, vilket gör dig till en strukturerad problemlösare samtidigt som du är öppen och en god kommunikatör på alla nivåer inom organisationen.

Inom Oriola Corporation arbetar vi enligt Lean vilket innebär att du förväntas bidra med förbättringsförslag för verksamheten, aktivt bidra till genomförandet av överenskomna förslag samt har en vana av att arbeta med ständiga förbättringar.

Du sympatiserar med företagets värderingar genom att vara öppen i din kommunikation, tar egna initiativ, är ansvarsfull, arbetar tillsammans i team och implementerar värderingarna i ditt dagliga arbete.

Tjänsten är en tillsvidareanställning med omgående start, placerad på vår anläggning i Fyrislund, Uppsala. Sista ansökningsdag är den 2020-02-23.

Vill du veta mer om tjänsten är du välkommen att kontakta Platschef Tove Kärvin på telefon 070-6696357. Intervjuer sker löpande under hela ansökningstiden.


Inför rekryteringsarbetet har vi tagit ställning till rekryteringskanaler och marknadsföring. Vi undanber oss därför bestämt kontakt med mediasäljare, rekryteringskonsulter och liknande. Visa mindre

Engineering Manager

Ansök    Aug 18    I.A.R. Systems AB    Utvecklingschef
IAR Systems is a knowledge-intensive and value-driven truly global company at the top of our industry. We have been providing world-leading software for building embedded applications for more than 35 years, and today over 150,000 developers are using our software. We supply the tools and services that make embedded systems development fast, efficient, and reliable, enabling our customers worldwide to deliver better products to their markets faster. About ... Visa mer
IAR Systems is a knowledge-intensive and value-driven truly global company at the top of our industry. We have been providing world-leading software for building embedded applications for more than 35 years, and today over 150,000 developers are using our software. We supply the tools and services that make embedded systems development fast, efficient, and reliable, enabling our customers worldwide to deliver better products to their markets faster.
About the role
As an Engineering Manager at IAR Systems, you will support the success of a team of 10-20 skilled and experienced software engineers, where you communicate expectations, initiatives, and goals. You will be part of the engineering management team and actively contribute to the continuous development of the department. In this role, you will also have close contact and collaborate with stake holders across various domains, such as project leaders and product managers.
You will be responsible for budgeting, and managing employees through the full employee journey of hiring, mentoring, performance and salary reviews, and exits. You will be responsible for your team’s outcomes, and for coaching your team to continuously deliver value to the stake holders and working towards the company’s goals.
You will report to the Director of Engineering and will be located in Uppsala.
Your qualifications and experience
You have some previous management experience with the know-how and ability to do what is needed to plan and uphold project plans, and deliver accordingly. As a manager of experienced engineers, a solid background in software engineering is a must so that you’re able to challenge and coach your team members in a collaborative, delivery-focused environment. Experience to advocate and advance modern software engineering practices is a prerequisite for the role. You are fluent in Swedish and English in both writing and speaking.
Communication is your most important tool. You will build and inspire your team by enabling a creative and challenging atmosphere. To be successful in this role, we believe you will bring a positive attitude, have the ability to deliver and receive constructive feedback, and gain the trust of your team.
Your application will receive extra credit if you have experience with DevOps, Cloud platforms, and Linux. In addition, it is a bonus if you have domain knowledge in any of the areas of microprocessor architecture, embedded systems, hardware-oriented development, or software development tools, such as compilers, debuggers, IDE, etc.
What are we offering?
You will be part of a multi-cultural and global business in a fast growing industry, an organization where every co-worker’s individual role is very important in the big picture. We are welcoming, open to new ideas, and take pride in our achievements. We offer you the opportunity to work in a curious, knowledge-sharing environment with a strong team spirit, where we will support you to grow both professionally and as an individual. We are problem-solvers and take on new challenges with excitement and energy. This is why we place great emphasis on your personal qualities and their alignment with our values.
Are you the person we are looking for? Please send us your application with cover letter and resume/CV today, and indicate “Engineering Manager” in the subject line. Selection and interviews will take place on a continuous basis and the post may be filled before the closing date, so please apply as soon as possible.
Questions? If you have any questions, please turn to Susanne Dahlén, Director of Engineering, at [email protected]
Applications are to be sent to [email protected] Visa mindre

Industrial Project Manager to Galderma

Ansök    Dec 19    Nestle    Utvecklingschef
Do you want to be part of a business that contributes to human health and well-being. Do you want to work as industrial project manager in a global organization that is currently in an exciting and expansive phase? Then this can be the role for you! Our Operations Project Management group at Galderma in Uppsala manages engineering & investment projects for medical device and pharmaceutical products within the Aesthetics area. We are now strengthening our g... Visa mer
Do you want to be part of a business that contributes to human health and well-being. Do you want to work as industrial project manager in a global organization that is currently in an exciting and expansive phase? Then this can be the role for you!
Our Operations Project Management group at Galderma in Uppsala manages engineering & investment projects for medical device and pharmaceutical products within the Aesthetics area.
We are now strengthening our group by looking for Industrial Project Managers.

About the role

As Industrial Project Manager will you provide day-to-day project management leadership to Industrialization project teams in the Operations Group. You will in close collaboration with other functions within the company drive the Operations development and improvements. This will ensure long-term capability of efficient supply of quality products to our customers and contributes to Galdermas short- and long-term growth.

As Industrial Project Manager, you will:

* Be accountable for project objectives, deliverables, timeline and budget
* Be responsible for developing and communicating project strategies, vision and goals
* Assess project risks with the project team, propose and follow-up mitigation and contingency plans 
* Manage site cross-functional teams of professionals responsible for Engineering, Operations, site infrastructure and facilitate cross-functional collaboration
* Ensure appropriate reporting of project progression inside and outside the team

About you

We believe that you have a university degree within, engineering, business or science. You have experience as project manager, with specific experience from the pharmaceutical/medical device industry is an advantage. You are used to working in an international environment.

We think that you have the following skills and competences:

* Good skills in project management tools and practices
* Good communication skills, both oral and written communication
* Good team leadership skills
* Good financial knowledge
* Experience in change management

We also believe that you are courageous, ambitious and goal-oriented. You know how to influence others and you have integrity and an open mind.

What we offer in return

As Galderma’s Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from early development to production and marketing. Here our 470 employees work on our world leading brands such as Restylane®, Azzalure® and Sculptra®.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala, only a 10-minute bike ride from Uppsala central station.

Your application

We welcome your application (CV and letter) via our company website www.galderma.com/job-search. You will be able to create a personal account and upload your application documents. Apply as soon as possible though no later than 19th of January.

Should you have questions about this opportunity you are welcome to contact Per-Olov Wedin, Head of Operations Project Management, on +46 73 387 1406.

 

About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com. Visa mindre

Senior Project Manager till Galderma

Ansök    Dec 20    Nestle    Utvecklingschef
Galderma is the world's largest independent global dermatology company.  Our Global Center of Excellence for Aesthetics is located in Uppsala, Sweden. Our Global Project Management department manages product development projects for medical device and pharmaceutical products within the Aesthetics area.   About the role As Senior Project Manager, will you provide day-to-day project management to global drug/medical device development project teams in the... Visa mer
Galderma is the world's largest independent global dermatology company.  Our Global Center of Excellence for Aesthetics is located in Uppsala, Sweden. Our Global Project Management department manages product development projects for medical device and pharmaceutical products within the Aesthetics area.

 

About the role

As Senior Project Manager, will you provide day-to-day project management to global drug/medical device development project teams in the Aesthetics Global Business Unit. In close collaboration with other functions within the company, you will drive the Aesthetics innovation pipeline progression to ensure timely supply of quality products to our customers and contribute to Galderma’s short- and long-term growth.

 

As Senior Project Manager, you will:
* Manage global cross-functional teams of professionals responsible for product development from early stage until launch
* Be accountable for project objectives, deliverables, timeline and budget
* Manage project decision making
* Be responsible for developing and communicating strategies, goals and long-term vision for projects
* Implement and organize actions to improve team motivation and shared understanding
* Ensure and facilitate cross-functional collaboration
* Assess project risks with the project team, propose and follow-up mitigation and contingency plans 
* Ensure appropriate reporting of project progression inside and outside the team
* Issue the project core documentation

 

About you

We believe that you have a university degree within science, engineering or business. You have at least 5 years of experience as project manager, with specific experience from the pharmaceutical industry including clinical development. You are used to working in an international environment.

 

We think that you have the following skills and competences:
* Excellent skills in project management tools and practices
* Excellent communication skills, both oral and written communication
* Good team leadership skills
* Good financial knowledge
* An analytical and strategic mindset
* Experience in change management

We also believe that you are courageous, ambitious and goal-oriented. You know how to influence others and you have integrity and an open mind.

What we offer in return

As Galderma’s Global Center of Excellence for Aesthetics, we have in Uppsala a unique edge as we have on our site the whole product chain from development to production and marketing. Here our nearly 450 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.

Your application

We welcome your application (resume and cover letter) via our company website www.galderma.com/job-search. You will be able to create a personal account and upload your application documents. Apply as soon as possible though no later than January 10, 2020. The selection process is ongoing.

Should you have questions about this opportunity you are welcome to contact Malin Johansson, Global Head of Project Management, on +46 73 387 1498.

We look forward to receiving your application!

About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com. Visa mindre

Product Life Cycle Manager to Galderma

Ansök    Dec 12    Nestle    Utvecklingschef
Are you interested in being at the centre of a production plant in an international organisation? Do you like being in contact with many different people in various functions? Are you detailed oriented but at the same time good at seeing the big picture? Then this is the role for you!   Galderma’s Aestetic business in Uppsala is looking for a Product Life Cycle Manager (PLCM) on a permanent basis.   As PLCM, you will be a member of the Product Lifecycl... Visa mer
Are you interested in being at the centre of a production plant in an international organisation? Do you like being in contact with many different people in various functions? Are you detailed oriented but at the same time good at seeing the big picture? Then this is the role for you!

 

Galderma’s Aestetic business in Uppsala is looking for a Product Life Cycle Manager (PLCM) on a permanent basis.

 

As PLCM, you will be a member of the Product Lifecycle Management (PLM) team, which is part of the Supply Chain department in the Galderma Uppsala Manufacturing division. PLM is made up of seven employees whereof four (including you) are PLCMs. Due to an increasing business world-wide we now have a vacant position giving you the opportunity to get new experiences and contribute to the group deliveries and development in an evolving organisation.

 

About the role

You are the Change leader for Change Control (CC’s) tasks related to labelling changes requested or required to the product assortment;
* You administer and coordinate change controls according to our SOPs
* You develop strategies related to the change controls being managed to ensure and drive the most efficient implementation of these change controls

You are the 1st shipment readiness leader
* You ensure that the supply chain planning, procurement and regulatory departments are informed of the impact of relevant changes that will affect their activities.
* You ensure that there is a 1st shipment readiness plan that is agreed, updated and communicated within the Uppsala organisation as well as with relevant affiliates on a regular basis
* Participate in projects with new/change of product and act as interface for the supply chain functions

You are the Master data leader
* You manage and ensure that product data within the Galderma item database systems is current and up to date.

About you

To be successful in the role:
* You have a university degree and/or long experience from the pharmaceutical or the biotech industry
* You have experience of managing change controls in a Good Manufacturing Practice (GMP) environment and it is an advantage if you also have experience working withTrackWise and the ERP system SAP or M3.
* You have experience in and appreciate the importance of adhering to a Quality management system
* You are proactive in pursing issues and finding pragmatic solutions when required 
* You are target oriented and show initiative, anticipate varying scenarios in order to ensure supply demands are met in a timely manner
* You show good leadership qualities and are highly organised.
* You bring excellent time management skills and are meticulous in your approach to pay attention to detail when required at the same time as you know how to drive activities forward at a required pace without getting entangled in the details
* You are proficient in both Swedish and English (oral and written communication)

What we offer in return

This position offers you an exciting, dynamic and challenging role with excellent opportunities for further personal development within our company.

As Galderma’s Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 450 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.

Your application

We welcome your application (CV and letter) via our company website http://www.galderma.com/job-search Apply as soon as possible though no later than January 10, 2020. The selection process is ongoing.

Should you have questions about this opportunity you are welcome to contact recruiting manager Angelica Hall, Manager Product Lifecycle Management: + 46 733 871508 or [email protected]

About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com. Visa mindre

Head of Global Medical and Scientific Experts to Galderma

Ansök    Dec 6    Nestle    Utvecklingschef
Do you want to be part of the largest independent company focused on dermatology? Do you want to be a key driver for the Galderma Aesthetic Global Medical Affairs Strategy? Then this can be the role for you! The Global Medical Affairs department in Uppsala, Sweden, is responsible for providing specialist medical and scientific support to Healthcare Professionals (HCPs) and Galderma staff. We are directly involved in the strategic discussions and decision-m... Visa mer
Do you want to be part of the largest independent company focused on dermatology? Do you want to be a key driver for the Galderma Aesthetic Global Medical Affairs Strategy? Then this can be the role for you!
The Global Medical Affairs department in Uppsala, Sweden, is responsible for providing specialist medical and scientific support to Healthcare Professionals (HCPs) and Galderma staff. We are directly involved in the strategic discussions and decision-making regarding new data generation, publications and other forums for sharing of information about our aesthetic products or best practices. Our work is focused on four areas: medical education and training, publications, clinical studies (Phase IV and IITs), pipeline and global medical affairs strategy.

About the role

As Head of Global Medical and Scientific Experts, you will lead the medical and scientific strategy of the Medical Affairs department for the aesthetics business unit (GBU). Reporting to the Global Head of Medical Affairs, you will be the manager for a team of three Medical Science Advisors. In addition and as a senior resource, you will provide medical insight and support of the Aesthetics GBU activities, both internal and external. The role is located in Uppsala, Sweden and can require about 25% of travel.

As Head of Global Medical and Scientific Experts, your main responsibilities will include:

 
* serving as the key medical resource and lead for the Medical Science Advisors, members of the Phase IV clinical team, and the study strategy and publication team
* serving as the lead for management of Investigator Initiated Studies (IISs)
* liaising closely cross functionally to ensure strong strategic support
* performing review and presentation of clinical data to support publications, claims and other medical affairs activities
* reviewing promotional material
* key Medical Affairs interface with the Safety, Regulatory, Clinical Development and Quality teams
* managing resources and priorities for your team

 

About you

* You have a PhD or MD with a strong preclinical background
* You are fluent in English (written and oral)
* Minimum of 7 years in a global pharmaceutical and/or medical device company in Medical Affairs and Clinical Development
* Demonstrated experience working cross-functionally and building alignment among stakeholders
* Demonstrated experience and working knowledge of international regulations and GCP of medical device and/ or pharmaceuticals
* Demonstrated experience in developing protocols, and conducting phase IV studies; experience in Medical Affairs study strategy
* Demonstrated experience in critically reviewing and analyzing scientific data, and have demonstrated ability to outline and write scientific papers and compile regulatory and technical documents
* Prior leadership experience of guiding teams is preferred

What we offer

As Galderma’s Global Center of Excellence for Aesthetics, we have in Uppsala a unique edge as we have on our site the whole product chain from early development to production and marketing. Here our 450 employees work on our world leading brands such as Restylane®, Azzalure® and Sculptra®.

We are offering you the opportunity to work in a fast growing and international environment, where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala, only a 10-minute bike ride from Uppsala central station.

 

Your application

We welcome your application in English (CV and letter) via our company website www.galderma.com/job-search. Apply as soon as possible though no later than January 15, 2020. The selection process is ongoing. We look forward to reading your application!

Should you have questions about this opportunity you are welcome to contact the HR department on [email protected]

We wish to inform you that Galderma can conduct pre-employment security checks for specific positions or activities. This security screening is performed by an external supplier after approval from applicants.

About Galderma

Galderma, the world's largest independent global dermatology company, was created in 1981 and is now present in over 100 countries with an extensive product portfolio to treat a range of dermatological conditions. The company partners with health care practitioners around the world to meet the skin health needs of people throughout their lifetime. Galderma is a leader in research and development of scientifically defined and medically proven innovative solutions for the skin. For more information, please visit www.galderma.com. Visa mindre

Ledare för Design Engineering & Senior Projektledare

Vill du arbeta på ett företag i framkant med modern teknologi? Bolaget driver samarbeten med stora dynamiska globala bolag samt levererar till kunder över hela världen. De globala bolagen är bl a verksamma inom diagnostik, halvledarindustri och avancerade optiska mätningar. Huvudkontor samt anläggning för utveckling och produktion finns i Upplands län. Om uppdraget Denna roll är en kombinerad roll som ledare för avdelningen Design Engineering och ... Visa mer
Vill du arbeta på ett företag i framkant med modern teknologi? Bolaget driver samarbeten med stora dynamiska globala bolag samt levererar till kunder över hela världen. De globala bolagen är bl a verksamma inom diagnostik, halvledarindustri och avancerade optiska mätningar.

Huvudkontor samt anläggning för utveckling och produktion finns i Upplands län.





Om uppdraget

Denna roll är en kombinerad roll som ledare för avdelningen Design Engineering och samtidig Senior projektledare för ett eller flera av våra absolut viktigaste produkt- och industrialiseringsprojekt.

Bolaget har som plan att expandera och som en del av detta kommer utvecklingsavdelningen att bestå av två olika delar, en innovation/R&D del och en del som ansvarar för utveckling, färdigställande av produkter samt att driva kundanpassade projekt.

Tjänsten vi erbjuder är i ett teknikområde som innehåller ett stort mått av nytänkande och där det inte alltid finns färdiga lösningar för uppgifterna. Här har du en unik möjlighet att själv kunna ta fram idéer kring koncept och att initialt själv vara med i det praktiska framtagandet av produkter. Vi arbetar i en spännande internationell miljö där resor förekommer. Vår strävan är att alltid vara den som snabbast levererar en fungerande lösning till kunden.

Är du den vi söker?

Vi söker dig med en Civilingenjörsexamen, gärna inom maskin, material eller teknisk fysik. Du har god kunskap och förståelse inom elektronik och mjukvara, gedigen erfarenhet av produktutveckling samt projektledning. Vi ser att du har erfarenhet av att implementera utvecklings- och projektlednings-processer. Du har erfarenhet av att etablera en effektiv organisation som både kan driva egna produktprojekt, kundanpassade projekt samt stödja Innovation/R&D avdelningen med vissa utvecklingsresurser.

Vi söker dig som har erfarenhet kring att arbeta med globala bolag. Du har någon form av internationell erfarenhet, helst via arbete mot internationella kunder men gärna även genom arbete i andra länder alternativt i en internationell organisation. Det är meriterande med erfarenhet kring både utveckling av högvolymkomponenter och sub-system, gärna inom olika applikationsområden. Du har gärna någon typ av entreprenörserfarenhet, antingen genom arbete i en startup eller genom deltagande i etablering av ny verksamhet.

Personliga egenskaper

Dina drivkrafter och egenskaper innebär att du kan implementera en kultur med kundfokus, snabbhet, flexibilitet och öppenhet, en organisation där medarbetarna mår bra och är beredda att delegera ansvar men också är beredda att ta ansvar. Du tycker det är viktigt att ha roligt på jobbet i kombination med att du levererar ett stort värde.

Låter det intressant?

Låter detta intressant är du välkommen att kontakta Amanda Norstedt, [email protected], tel. 070-236 36 99 för mer information om tjänsten. Visa mindre

Senior Utvecklingsledare/Aktivitetsledare Product Assurance

Ansök    Nov 1    PHADIA AB    Utvecklingschef
I Sverige är vi cirka 1,000 Thermo Fisher Scientific anställda som jobbar ifrån fem siter och hemma kontor. På vår största site i Uppsala jobbar vi med utveckling, tillverkning och marknadsföring av allergi tester och diagnostiska system. I centrala Stockholm har vi två mindre kontor som förser våra kunder med life-science och analytiska instrument och produkter. På västkusten i Göteborg hittar ni vårt nybyggda Nordiska lager och kundsupport team som jobba... Visa mer
I Sverige är vi cirka 1,000 Thermo Fisher Scientific anställda som jobbar ifrån fem siter och hemma kontor. På vår största site i Uppsala jobbar vi med utveckling, tillverkning och marknadsföring av allergi tester och diagnostiska system. I centrala Stockholm har vi två mindre kontor som förser våra kunder med life-science och analytiska instrument och produkter. På västkusten i Göteborg hittar ni vårt nybyggda Nordiska lager och kundsupport team som jobbar med ett brett utbud av laboratorieprodukter. Bland åkrarna utanför Ängelholm jobbar teamet med att ta fram högkvalitativa allergena råvaror. I Sverige jobbar vi alltså brett och varierat, men delar alla samma mål - att kunna hjälpa våra kunder göra världen hälsosammare, renare och säkrare.
Division och introduktion - IDD
Du kommer att vara en del av Thermo Fisher Scientific, ImmunoDiagnostics Division (IDD), som utvecklar, tillverkar och marknadsför diagnostiska test för allergi, astma och autoimmuna sjukdomar. Med 1700 anställda globalt är IDD världsledande inom invitrodiagnostik (IVD) av allergi och ledare inom autoimmundiagnostik i Europa. I Uppsala, med cirka 700 medarbetare, finns divisionens största site med både utveckling och tillverkning.
Vi söker en drivande person med gedigen erfarenhet av aktivitetsledning och produktvårdsaktiviteter till gruppen Product Assurance som ingår i avdelningen Product Quality. Tjänsten är en tillsvidareanställning.
Hur kommer du kunna påverka?
Gruppen Product Assurance består av 8 medarbetare och tillhör avdelningen Product Quality inom Operations. Gruppen ansvarar för att utreda och hantera process-, produkt- och akuta råvaruavvikelser, kontrollera valideringsråvaror och samt hantera långsiktiga åtgärder för att säkerställa produktkvalitet. Gruppen har även konstruktions- och försörjningsansvar för svampråvara.
Mer om jobbet
Rollen innebär ett stort ansvar och dina arbetsuppgifter kommer främst att vara:
• Initiera och driva ändringar för att upprätthålla befintlig produktkvalitet
• Driva egna eller delta i aktiviteter för att förbättra produktionsprocesser, exempelvis genom uppskalning eller utveckling av produkt
• Problemlösning och bidra med hjälp vid komplexa avvikelser
• Handledning och upplärning av ny personal
• Representera gruppen i olika forum
Tjänsten innebär att hitta förebyggande och långsiktiga åtgärder för att säkerställa produktkvalitet och produktens möjlighet till uppskalning och producerbarhet. Arbetet innefattar hela kedjan från att självständigt designa försöksupplägg, praktiska laborativa försök, analys av resultat och formulera och dokumentera dessa i utredningsrapporter, föreslå åtgärder och hantera dessa enligt ändringshanteringsrutiner.
Vem söker vi?
Degree required and discipline
Vi ser gärna att du har högskoleutbildning inom kemi, teknisk biologi eller motsvarande och det är en fördel om du har erfarenhet av att jobba med aktivitetsledning.
Knowledge, Skills, Abilities
För att trivas i rollen är du en nyfiken, noggrann och drivande person. Du har god analytisk förmåga, tycker om problemlösning och är någon som vill förstå grundorsaker och hitta lösningar. Är van att ta egna initiativ, prioritera och planera ditt eget arbete som du bedriver effektivt, systematiskt och analytiskt. Du också ha lätt för att kommunicera och samarbeta i team.
Är du intresserad?
Letar du efter ett meningsfullt jobb på ett internationellt företag som har starka värderingar? Vill du ha ett varierande jobb med eget ansvar där du verkligen kan göra en skillnad i människors vardag? Om detta låter intressant så kan du vara den personen vi söker!
SÖK NU via vår karriärsida https://jobs.thermofisher.com/
Har du frågor kontaktar du: Monica Norén, Gruppchef Product Assurance, 018 163 892, [email protected] eller Senior Recruiter, Anja Soh Dyppel, [email protected] Visa mindre

Business Development & Alliance Manager

Ansök    Mar 22    Nestle    Utvecklingschef
Do you want to be part of a business that contributes to human health and well-being? Do you want to work as a Business Development & Alliance Manager in a global organization that is in an expansive phase? Then this can be the role for you!   The Business Development Department in Uppsala is responsible for driving and executing business development and alliance activities for our Aesthetic global unit.   About the role Reporting to the Global Head of... Visa mer
Do you want to be part of a business that contributes to human health and well-being? Do you want to work as a Business Development & Alliance Manager in a global organization that is in an expansive phase? Then this can be the role for you!

 

The Business Development Department in Uppsala is responsible for driving and executing business development and alliance activities for our Aesthetic global unit.

 

About the role
Reporting to the Global Head of Business Development, you will focus on managing existing strategic alliances and execute business development activities according to the company priorities and strategic plan.

 

As Business Development & Alliance Manager you will:
* Be the key point of contact for our strategic partners throughout the world
* Manage all aspects of alliances (business reviews, communication, coordination of resources, definition of governance, organization of meetings etc.)
* Manage licensing-in and licensing-out of products, technologies and related materials.
* Manage due diligence processes in coordination with other key departments
* Develop financial models together with finance partner
* Prepare all documents linked to relevant projects (business plan, presentation, secret note etc.)
* Identify and explore new business models and business opportunities to grow our business
* Research market conditions and developments including attendance of key congresses & meetings

 

To be successful in this role you will need to understand and effectively engage a wide range of internal and external functional areas including Legal, Finance, Development, Medical and Regulatory Affairs, Marketing and Project Management.

You are able to travel up to 30% including internationally.

 

About you

We believe that you have the following background:
* University degree in business administration or science.
* +15 years of experience gained in  management roles:
- Commercial positions with international exposure
- Business Development and/or Alliance Management
* Solid experience in and understanding of the pharmaceutical/device industry (aesthetics field preferred)

 

We also believe that you bring the following skills and competences:
* Very good business acumen and financial & negotiation skills
* Advanced Project management skills: you can work both on a strategic level and manage specific operations in a complex context
* Strong collaboration skills across functions and cultures and ability to manage stakeholders
* An analytical and strategic mindset
* Understand customer focus and brand focus
* Strong verbal and written communication and presentation skills in English

 

What we offer in return
As Galderma’s Global Center of Excellence for Aesthetics we have in Uppsala a unique edge as we have on our site the whole product chain from research and development to production and marketing. Here our nearly 450 employees work on our world leading brands such as Restylane, Azzalure and Sculptra.

 

We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located just by the river (Fyrisån) in Uppsala only a 10 minute bike ride from Uppsala Central Station.

 

Your application
We welcome your application (CV and letter in English) via our company website https://www.nestleskinhealth.com/job-search. Apply as soon as possible though no later than April 10, 2019. The selection process is ongoing.

Should you have questions about this opportunity you are welcome to contact Daniel de Boer, Global Head of Business Development, on [email protected]

 

We inform candidates that the company may perform a background control as part of the final recruitment step.

 

About the company
Galderma is a global leader in medical solutions for the skin, hair and nails, wholly-owned by Nestlé Skin Health, a subsidiary of Nestlé. The company has been developing its extensive range of medically-proven solutions since its creation in 1981. It exclusively partners with healthcare professionals to target a variety of dermatological conditions and skin needs.

Headquartered in Lausanne, Switzerland, Galderma has more than 5,500 employees and 35 affiliates around the world. Its products are distributed in over 100 countries. Its development centers and manufacturing facilities are dedicated to providing a wide range of innovative and science-based medical solutions to meet the highest standards of safety and efficacy. Visa mindre

Director of Quality and Regulatory to C - RAD

Director of Quality and Regulatory Are you interested in making an impact in the area of radiation therapy and help new products reach the market? Do you want to help patients around the world to get more efficient radiation therapy? C-RAD is looking for their next Director with assignments within quality control, quality assurance and regulatory affairs. C-RAD works within the field of radiation therapy and are trying to improve among other things re... Visa mer
Director of Quality and Regulatory
Are you interested in making an impact in the area of radiation therapy and help new products reach the market? Do you want to help patients around the world to get more efficient radiation therapy? C-RAD is looking for their next Director with assignments within quality control, quality assurance and regulatory affairs.



C-RAD works within the field of radiation therapy and are trying to improve among other things real time monitoring of radiation therapy.



Job description

You will implement and maintain Quality Systems for C-Rad global quality and regulatory systems in compliance with US Food and Drug Administration, ICH and international requirements, and will lead the strategic and operational aspects of C-Rad’s quality and regulatory program. You are responsible for the Quality Control and Quality Assurance functions and ensure compliance to corporate policies, US FDA, other applicable federal/state agency and international requirements, as appropriate. You also lead the preparation and submission of regulatory documents in the US and other countries for approval at various stages of the submission process. You will be the contact point towards the FDA, EU and other regulatory agencies.



Other common tasks will be:

- Conducting internal and external audits.

- Manage supplier quality and contract manufacturing quality.

- You will be the global quality representative within the company.

- Provide regulatory training and foster a corporate commitment to quality.



Qualifications

For this role we see a person who has worked within the field of medical or biological devices. You probably have an bachelor’s degree in engineering, science or other relevant field. Have you also had experience with the FDA and been the lead auditor then this job will suit you. In this role we give you the opportunity to work in a wide range of tasks from implementing a quality system to training the employees and assure quality compliance. As a person we see this employee as an:



- Collaborative person that puts the companies goals first.

- Ability to engage colleagues and keep a positive attitude

- Listen attentively to colleagues and other collaboration partners.



There will be travels less than 20 % of the time. It is important for us to see that all of the competencies in the market. We welcome all candidates.



Application: Please apply before 2019-04-28 In this recruitment selection will take place continuously. Please send in your application today!



Contact information: In this recruitment C-RAD has decided to collaborate with Dfind Science & Engineering. Please contact Jenny Davidsson [email protected] for any questions concerning this position. Visa mindre

Director of Quality and Regulatory to C - RAD

Kvalitetschef Are you interested in making an impact in the area of radiation therapy and help new products reach the market? Do you want to help patients around the world to get more efficient radiation therapy? C-RAD is looking for their next Director with assignments within quality control, quality assurance and regulatory affairs. C-RAD works within the field of radiation therapy and are trying to improve among other things real time monitoring of... Visa mer
Kvalitetschef
Are you interested in making an impact in the area of radiation therapy and help new products reach the market? Do you want to help patients around the world to get more efficient radiation therapy? C-RAD is looking for their next Director with assignments within quality control, quality assurance and regulatory affairs.



C-RAD works within the field of radiation therapy and are trying to improve among other things real time monitoring of radiation therapy.



Job description

You will implement and maintain Quality Systems for C-Rad global quality and regulatory systems in compliance with US Food and Drug Administration, ICH and international requirements, and will lead the strategic and operational aspects of C-Rad’s quality and regulatory program. You are responsible for the Quality Control and Quality Assurance functions and ensure compliance to corporate policies, US FDA, other applicable federal/state agency and international requirements, as appropriate. You also lead the preparation and submission of regulatory documents in the US and other countries for approval at various stages of the submission process. You will be the contact point towards the FDA, EU and other regulatory agencies.



Other common tasks will be:

- Conducting internal and external audits.

- Manage supplier quality and contract manufacturing quality.

- You will be the global quality representative within the company.

- Provide regulatory training and foster a corporate commitment to quality.



Qualifications

For this role we see a person who has worked within the field of medical or biological devices. You probably have an bachelor’s degree in engineering, science or other relevant field. Have you also had experience with the FDA and been the lead auditor then this job will suit you. In this role we give you the opportunity to work in a wide range of tasks from implementing a quality system to training the employees and assure quality compliance. As a person we see this employee as an:



- Collaborative person that puts the companies goals first.

- Ability to engage colleagues and keep a positive attitude

- Listen attentively to colleagues and other collaboration partners.



There will be travels less than 20 % of the time. It is important for us to see that all of the competencies in the market. We welcome all candidates.



Application: Please apply before 2019-04-24. In this recruitment selection will take place continuously. Please send in your application today!



Contact information: In this recruitment C-RAD has decided to collaborate with Dfind Science & Engineering. Please contact Jenny Davidsson [email protected] for any questions concerning this position. Visa mindre