Lediga jobb Double Bond Pharmaceutical AB i Uppsala

Double Bond Pharmaceutical is looking for QA Specialist with experience in the pharmaceutical sector.
You will be responsible for ensuring that the products' life cycles are of good high quality and meet special requirements.
Your duties may include:
- Quality control procedures, Ccoordinate and conduct investigations, deviations, and CAPA
- Participate in (external) audits
- Plan and carry out internal audits
- Review documentation (protocols, SOPs, …)
- Approve validations and qualifications
- Stay up to date with industry trends and best practices in quality assurance and regulatory requirements.
- Manage and develop internal processes and ensure that these meet both internal and external requirements
- Support the development team with review and quality assurance
- Assist the manufacturing department
- support QC, if necessary

About you: to succeed in the role of QA specialist, we see that you have:
- University or college education of at least 4 years with a scientific focus such as biotechnology, biology, chemistry, biomedicine, or pharmacy
- At least 1 year experience of work experience in the role of QA or equivalent
- Knowledge of product development in the pharmaceutical industry
- Good knowledge of regulatory documentation and requirements, qualification, and validation in the EU (mandatory). Outside of the EU would be a merit.
- Ability to work according to GMP and LEAN
- English fluent (Swedish would be a merit)
- Experience in documenting and knowledge of MS Office
- As a person, you work in a structured way and have a strong drive for quality work
- You are easy to communicate with while being accurate and analytical. You work just as well independently as in collaboration with others. Furthermore, you are motivated by achieving set goals and are happy to celebrate this together with your colleagues.
To succeed in this service, it is of utmost importance that you are an analytical, structured, and quality-conscious person. You are communicative, confident in yourself and your skills and thus have no problems pursuing issues within the organization in accordance with the internal and external requirements that have been established. Your way of working is permeated by structure and accuracy with a high degree of commitment.
Other information:
Start: ASAP
Scope: part-time (50-100% can be negotiated)
Working hours: office hours
Location: Uppsala (office based)
Salary: By agreement

We recommend that you submit your application immediately as we make an ongoing selection.
Please send your personal letter and CV to Georg Kalbin at [email protected]
Please indicate if you have work permit for Sweden.

About Double Bond Pharmaceutical (DBP) AB, Uppsala-Sweden:
DBP develops innovative first-in-class approaches for the treatment of cancers, infections, autoimmune diseases, and other life-threatening disorders. Our mission is to provide patients with more efficient and safe products in areas where their needs are unmet.
DBP’s team has international and ambitious young experts in all relevant areas to successfully reach the market.
DBP has a bottom-up organization, allowing each individual member to contribute significantly to every project. As a small company, we collaborate closely with all departments, quickly adaptable and reactive to changes.
We are committed to delivering high-quality products to our partners and customers, and we prioritize excellence in every aspect of our operations. Visa mindre

Clinical Development Manager
Double Bond Pharmaceutical is looking for Clinical Development Manager to join our team.
You will be responsible for
· Development of clinical documents such as protocol/amendment update, IB update, annual study report, etc;
· Contribute to regulatory activities such as IND, NDA submission, and data cleaning activity;
· Clinical interface for other functions for successful delivery of study;
· Identify and qualify possible clinical trial sites;
· Build relationships to gain market advantage including thought leaders and principal investigators;
· Vendor management – Identify suitable vendors, delegate vendor responsibilities, develop vendor reporting procedures and plan of action.
About you: to succeed in the role of Clinical development manager, we see that you have:
· University or college education of at least 4 years with a scientific focus such as biotechnology, biology, chemistry, biomedicine, or pharmacy
· At least 1-year experience of work experience in the field of clinical trials
· Knowledge of product development in the pharmaceutical industry
· Knowledgeable in science of oncology and able to analyze the data
· Good knowledge of regulatory documentation and requirements
· Ability to work according to GXP and LEAN
· English fluent (Swedish would be a merit)
· Experience with working according to GCP/ICH guidelines;
· Experience in documenting and knowledge of MS Office
· As a person, you work in a structured way, have a strong drive for quality work and demonstrate a considerable degree of autonomy
· You are easy to communicate with while being accurate and analytical. You work just as well independently as in collaboration with others. Furthermore, you are motivated by achieving set goals and are happy to celebrate this together with your colleagues.
To succeed in this position, it is of utmost importance that you are an analytical, structured, and quality-conscious person. You are communicative, confident in yourself and your skills and thus have no problems pursuing issues within the organization in accordance with the internal and external requirements that have been established. Your way of working is permeated by structure and accuracy with a high degree of commitment.
Other information:
Start: ASAP
Scope: full-time
Working hours: office hours
Location: Uppsala (office based)
Salary: By agreement

We recommend that you submit your application immediately as we make an ongoing selection.
Please send your personal letter and CV to Georg Kalbin at [email protected]

About Double Bond Pharmaceutical (DBP) AB, Uppsala-Sweden:
DBP develops innovative first-in-class approaches for the treatment of cancers, infections, autoimmune diseases, and other life-threatening disorders. Our mission is to provide patients with more efficient and safe products in areas where their needs are unmet.
DBP’s team has international and ambitious young experts in all relevant areas to successfully reach the market.
DBP has a bottom-up organization, allowing for each individual member to contribute significantly to every project. As a small company, we have a close collaboration between all departments, quickly adaptable and reactive to changes. Visa mindre

Double Bond Pharmaceutical is looking for QA Specialist with experience in the pharmaceutical sector.
You will be responsible for ensuring that the products' life cycles are of good high quality and meet special requirements.
Your duties may include:
- Quality control procedures, Ccoordinate and conduct investigations, deviations, and CAPA
- Participate in (external) audits
- Plan and carry out internal audits
- Review documentation (protocols, SOPs, …)
- Approve validations and qualifications
- Stay up to date with industry trends and best practices in quality assurance and regulatory requirements.
- Manage and develop internal processes and ensure that these meet both internal and external requirements
- Support the development team with review and quality assurance
- Assist the manufacturing department
- support QC, if necessary

About you: to succeed in the role of QA specialist, we see that you have:
- University or college education of at least 4 years with a scientific focus such as biotechnology, biology, chemistry, biomedicine, or pharmacy
- At least 1 year experience of work experience in the role of QA or equivalent
- Knowledge of product development in the pharmaceutical industry
- Good knowledge of regulatory documentation and requirements, qualification, and validation in the EU (mandatory). Outside of the EU would be a merit.
- Ability to work according to GMP and LEAN
- English fluent (Swedish would be a merit)
- Experience in documenting and knowledge of MS Office
- As a person, you work in a structured way and have a strong drive for quality work
- You are easy to communicate with while being accurate and analytical. You work just as well independently as in collaboration with others. Furthermore, you are motivated by achieving set goals and are happy to celebrate this together with your colleagues.
To succeed in this service, it is of utmost importance that you are an analytical, structured, and quality-conscious person. You are communicative, confident in yourself and your skills and thus have no problems pursuing issues within the organization in accordance with the internal and external requirements that have been established. Your way of working is permeated by structure and accuracy with a high degree of commitment.
Other information:
Start: ASAP
Scope: part-time (50-100% can be negotiated)
Working hours: office hours
Location: Uppsala (office based)
Salary: By agreement

We recommend that you submit your application immediately as we make an ongoing selection.
Please send your personal letter and CV to Georg Kalbin at [email protected]

About Double Bond Pharmaceutical (DBP) AB, Uppsala-Sweden:
DBP develops innovative first-in-class approaches for the treatment of cancers, infections, autoimmune diseases, and other life-threatening disorders. Our mission is to provide patients with more efficient and safe products in areas where their needs are unmet.
DBP’s team has international and ambitious young experts in all relevant areas to successfully reach the market.
DBP has a bottom-up organization, allowing each individual member to contribute significantly to every project. As a small company, we collaborate closely with all departments, quickly adaptable and reactive to changes.
We are committed to delivering high-quality products to our partners and customers, and we prioritize excellence in every aspect of our operations. Visa mindre

SCIENTIFIC BUSINESS DEVELOPMENT MANAGER
Would you wish to use your drug discovery and development experience in a more business-oriented way in the pharmaceutical industry– and earn while learning? Double Bond Pharmaceutical is looking for a Scientific Business Development Manager. An advanced degree and some industry experience in discovery (biology or chemistry) or preclinical development are required. Do you already have BD experience? So, please read the info below because you may be the right person.
The role provides an opportunity for a highly-motivated individual to work in managing several projects together with partners (CROs, consulting firms), interface with R&D scientists (internally and externally), and with the CEP as part of a collaborative team. Roles such as this can be an excellent path to more business-related positions in life science organizations. To be considered you should be an eager learner, enjoy working with people, be great at communication, and like a fast-paced, multi-faceted environment. You also should have:
MS or Ph.D. with 1-year experience in the pharmaceutical/biotech industry in a scientific or BD role
Strong skills in communication and relationship building
Drive and independence while also learning from, supporting, and sharing information with other team members
Ability to manage a project including deliverables, timelines, etc., and coordinate efforts between multiple stakeholders (medicines agencies, CROs, universities…)
Abilities to identify and solve problems, multitask, and learn

Preferably, also
Project management experience (a plus, but not necessary)
Experience and comfort with working with multiple cultures and nationalities
Swedish speaker


To apply
Send your resume & cover letter to Georg Kalbin ([email protected])
We look forward to your application! Visa mindre

Projektledare, från R&D till kommersialisering


Om Double Bond Pharmaceutical AB:
Double Bond Pharmaceutical är ett snabbväxande läkemedelsföretag beläget i Uppsala som utvecklar och kommersialiserar banbrytande metoder för riktad behandling av olika typer av cancer, infektioner, autoimmuna sjukdomar samt andra livshotande sjukdomar. Företagets främsta mål är att förse patienter och marknaden med mer effektiva och säkra produkter framförallt inom de områden där dessa behov inte har uppnåtts eller är starkt otillfredsställda. I vår strävan att utveckla läkemedel av högsta kvalité kombinerar vi redan väletablerade effektiva metoder med vår innovativa banbrytande teknologi för att erbjuda nya självnavigerande målstyrda terapeutiska möjligheter för behandling av livshotande sjukdomar. Vår vision är att utvecklas i så hög takt som möjligt och leverera bästa möjliga kvalité i utveckling av våra produkter.
Vårt dotterbolag, Drugsson AB riktar sig till att distribuera unika produkter på de nordiska samt icke reglerade marknaderna. Vi strävar efter att bli en utmanare i dessa marknader och ge patienterna högkvalitativa, effektiva och lättanvändbara produkter, för alla åldrar. Drugsson distribuerar in-licensierade, redan EU-registrerade produkter från våra partners / framtida partners.


Arbetsbeskrivning:
Projektledaren kommer främst att leda produkternas tillverkning, från labbskala, överföring till CMO till kommersialisering. Produkterna är komplexa och högprofilerade läkemedelsprodukter. Denna position är ansvarig för det operativa arbetet både internt och externt för att driva genomförandet av projektgrupperna. Projektledaren kommer att arbeta nära projektledarna för andra tvärfunktionella projektgruppmedlemmar såsom preklinisk och kliniska avdelningarna inom bolaget. Detta för att upprätta och underhålla projektplaner och budgetar, organisera och leda projektgruppsmöten, främja kommunikation och samordna mellan funktionella grupper. Denna position kommer att vara ansvarig för att säkerställa tillräcklig resurs för att uppfylla mål, identifiera risker / begränsningar och tillhandahålla projektstatusuppdateringar för att säkerställa att projektteamen når viktiga strategiska mål och i slutändan lyckas leverera banbrytande terapier till våra patienter.
Projektledaren förväntas även att leda arbetet över dotterbolagets verksamhet. Upprätthålla och underhålla CMC dokumentation (i form av IMPD och CTD) samt registrering av produkter (olika klassificeringar) enligt gällande krav. Detta arbete förväntas dock övertas med tiden och eventuella utbildningar kan komma att ges.


Uppdraget:
Arbetet fokuseras på att vara en flexibel, operativ projektledare som kan bidra till organisationen i den komplexa och reglerade GxP-miljön. Fungera som projektledare för tillverkningsavdelningen, samordna och samarbeta med andra avdelningar såsom prekliniska och kliniska avdelningar. Agera regleringsansvarig, registreringsansvarig och distributionsansvarig för dotterbolaget efter viss tid. Arbetet kräver mycket noggrannhet då man kommer att skriva och granska dokument inklusive vetenskapliga dokument.
Som projektledare kommer du att utföra och dokumentera allt operativt arbete enligt skriftliga interna rutiner. Var engagerad i utveckling och förbättring av interna processer och hantera avvikelser / leverantörsutvärderingar / förändringsplaner etc.


Profil:
- Universitetsexamen i biovetenskap, kemi, apotekare eller relaterat område krävs.
- Förstå disciplinerna inom läkemedelsproduktutveckling för att bidra till en effektiv organisation.
- Förmåga att arbeta i ett team, i en kulturellt diversifierad, komplex och föränderlig miljö mest internt men till viss del externt.
- Nyfiken och innovativ inställning med problemlösningsförmåga - lösa problem med minimal vägledning.
- Bra organisatoriska färdigheter för att hantera dokumentationsmaterial och informationsprocesser.
- Goda förhandlingsfärdigheter, aktivt lyssnande och relationshantering.
- Goda svenska och engelska språkkunskaper, både skriftligt och muntligt.
- Bra på tidshantering och analytiska färdigheter.
- Goda datakunskaper, Microsoft Office.


Som person är du:
Analytisk, noggrann, ansvarstagande, självgående och iniativtagande.


Annan information:
· Start: Snarast
· Varaktighet, arbetstid: Heltid, tillsvidare med 6 månaders provanställning
· Placering: Uppsala


Vi går igenom urvalet löpande och annonsen kan stängas ner innan tjänsten är tillsatt om vi gått över till urvals- och intervjufasen.


Vänligen skicka din CV och personliga brev till [email protected].
För mer information, kontakta Georg Kalbin nedan.
Georg Kalbin
[email protected]
tel. 073-5752019 Visa mindre

Quality Assurance (QA) Specialist (50%-100%)
Double Bond Pharmaceutical is looking for QA Specialist with experience in the pharmaceutical sector.
You will be responsible for ensuring that products' life cycles are of good quality and meet special requirements.
Your duties may include:
- Coordinate and conduct investigations, deviations, and CAPA
- Participate in (external) audits
- Plan and carry out internal audits
- Review documentation (protocols, SOPs, …)
- Approve validations and qualifications
- Manage and develop internal processes and ensure that these meet both internal and external requirements
- Support the development team with review and quality assurance
- Assist the manufacturing department
- support QC, if necessary

About you: to succeed in the role of QA specialist, we see that you have:
- University or college education of at least 4 years with a scientific focus such as biotechnology, biology, chemistry, biomedicine, or pharmacy.
- At least 1-year experience of work experience from the role of QA or equivalent
- Knowledge of product development in the pharmaceutical industry
- Good knowledge of regulatory documentation and requirements, qualification, and validation in the EU (mandatory). Outside of the EU would be a merit.
- Ability to work according to GMP and LEAN
- English fluent (Swedish would be a merit)
- Experience in documenting and knowledge of MS Office
- As a person, you work in a structured way and have a strong drive for quality work
- You are easy to communicate with while being accurate and analytical. You work just as well independently as in collaboration with others. Furthermore, you are motivated by achieving set goals and are happy to celebrate this together with your colleagues.
To succeed in this service, it is of utmost importance that you are an analytical, structured, and quality-conscious person. You are communicative, confident in yourself and your skills and thus have no problems pursuing issues within the organization in accordance with the internal and external requirements that have been established. Your way of working is permeated by structure and accuracy with a high degree of commitment.
Other information:
Start: ASAP
Scope: part-time (50-100% can be negotiated)
Working hours: office hours
Location: Uppsala (office based)
Salary: By agreement

We recommend that you submit your application immediately as we make an ongoing selection.
About Double Bond Pharmaceutical (DBP) AB, Uppsala-Sweden:
DBP develops innovative first-in-class approaches for the treatment of cancers, infections, autoimmune diseases, and other life-threatening disorders. Our mission is to provide patients with more efficient and safe products in areas where their needs are unmet.
DBP’s team has international and ambitious young experts in all relevant areas to successfully reach the market.
DBP has a bottom-up organization, allowing for each individual member to contribute significantly to every project. As a small company, we have a close collaboration between all departments, quickly adaptable and reactive to changes. Visa mindre

Product Development Assistant
Double Bond Pharmaceutical AB
We are curious, creative, and have new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join DBP and apply your expertise in a company that are following the science and turn ideas into life changing medicines. We have an exciting opportunity for a talented Scientist to be based in Uppsala, Sweden.
Our main business is within Drug Product Delivery within Pharmaceutical Development. We develop new investigational medicinal products and deliver high value to early phase clinical trials. We also support launched, pre-launched products under development within different therapeutic areas to the Nordic Market. Additionally, we distribute different product types mainly in Sweden. We work in a fast-paced environment where flexibility and agility enable us to deliver high value products to the market.
The Scientist role will be a flexible role within Drug Product Developments’ three operational skill areas: Development of new pharmaceutical products (according to GxP), Registration (regulatory affairs) and Distribution (according to GDP). We are looking to complement our existing team with a scientist.
Main Duties and Responsibilities:
The work is focused on being a flexible operational scientist who can contribute to the organization in the complex and regulated GxP environment. Act as an assistant to the product development team (manufacturing, pre-clinical and clinical departments), distribution manager, regulatory affairs manager and QA manager. To write and review documents including scientific documents.
As a scientist you will perform and document all the operational work according to written internal procedures. Be engaged in the development and improvement of internal processes and manage deviations/supplier evaluations/change plans etc.
Essential requirements and skills:
Newly graduated MSc in chemistry/pharmacy/engineering or equivalent experience.
Understanding the disciplines in Drug Product Development, Supply Chain and in order to contribute to an effective organization
Demonstrated ability to work with teams in a culturally diverse, complex and changing environment most internally but to some extent externally
Curious and innovative mindset with problem solving ability - resolve issues with minimal guidance
Good organizational skills to manage the documentation material and information processes
Good written and verbal English communication and understanding
Good written and verbal Swedish communication and understanding is a plus
Time management and analytical skills
Good computational skills, Microsoft Office


You will be trained in every aspect of the business with an introductory start. We deploy a great importance to social characteristics and attitude. As a person, you are ambitious, enterprising, and interested in actively contributing to our development and continued success, while you are humble and flexible and see opportunities rather than problems when you encounter obstacles and new tasks. Furthermore, you are a positive and social person with a lot of energy who thrives with an employer that is characterized by ambition, great community, and cohesion.
OTHER INFORMATION
· Start: As soon as possible, for the right person, notice period is taken into account
· Scope: Full-time, long-term assignment
· Location: Uppsala.
We review the selection on an ongoing basis; hence the position may be filled if we have moved on to the selection and interview phase. Please send in your CV together with your Personal Letter to [email protected]
For more information regarding the position, please contact:
Georg Kalbin
[email protected]
tel. 073-5752019 Visa mindre

Double Bond Pharmaceutical is a fast-growing pharmaceutical company located in Uppsala that develops and commercializes groundbreaking methods for targeted treatment of various types of cancer, infections, autoimmune diseases and other life-threatening illnesses. Our main goal is to provide patients and the market with more efficient and safe products, especially in the areas where these needs have not been met or are unsatisfactory. We believe that no treatment and medicine should be seen as a "luxury" and a treatment in itself should not cause any suffering to the patients. In our quest of developing medicines of the highest possible quality, we have already combined well-established effective methods with our innovative pioneering technology to offer new targeted therapeutic opportunities for the treatment of life-threatening diseases. We strive to deliver the best possible quality in the development of our products. In our company there are no restrictions when it comes to self-development and every employee has both ultimate freedom and ultimate responsibility for their part of the work. If you are ambitious, energetic, structured and meticulous, we would gladly see you as a potential member of our team today or sometime in the future.
About the service: We offer the job in different parts of the company's operations and we can offer challenging, fun and constantly evolving tasks for the right candidate. We work on the basis of trust, respect and responsibility. Our main working language is English, however, you will be also responsible for contacting our partners in Eastern Europe, so knowing Russian language is also considered as a requirement.
Who are you? You have a University degree, preferably a PhD, with a relevant specialty e.g. chemistry, pharmacy, biotechnology, engineering or similar and are interested in working in the pharmaceutical industry. You possess very good speaking and writing skills in both English and Russian and you have good computer skills. You are able to take responsibility, you are structured, organized and you are eager to take on new challenges. You can handle high tempo of working and you can work independently as well as in a team.


Requirements: 
- Very good knowledge of chemistry (organic / analytical or equivalent) or biology.
- Very good speaking and writing skills in English and Russian.
- Determination and ability to take responsibility. 
- Ability to work independently and as a team player.
- Experience in working with GMP guidelines.            
- Experience in product development projects, as well as preparing and updating documents.                      
- Experience of working in the pharmaceutical industry
- Experience of working in a multicultural team.
- Experience of working with analytical techniques.


Together with our ambitious and experienced team you will develop our products for the European and global market. Here, in Double Bond you will have a great opportunity for personal development and you will have a chance to work with interesting and challenging tasks every day. If you are interested in the job, please send your resume and cover letter to: [email protected]. Start time: immediately or by personal agreement. Visa mindre