Lediga jobb Q-Med AB i Uppsala

Vi söker nu en skicklig och engagerad Maintenance Engineer till vårt operationsteam i Uppsala, där avancerad teknik, högkvalitativ tillverkning och ett tydligt syftesdrivet innovationsfokus möts. I denna roll blir du en nyckelperson i att säkerställa stabil, säker och regelverksefterlevande produktion - och ditt arbete kommer att ha en direkt påverkan på produkter som används av patienter världen över.
Om du trivs med att arbeta nära produktionen, lösa tekniska utmaningar och ta ansvar i en reglerad miljö där kvalitet verkligen spelar roll, är detta en möjlighet du inte vill missa.

På Galderma erbjuder vi inte bara ett jobb - vi bjuder in dig att bli en del av något större. Som en global ledare inom dermatologi kombinerar vi syfte med innovation för att förbättra livet för miljontals människor.

Om Galderma

Galderma är en framväxande, renodlad kategoriledare inom dermatologi och finns representerat i cirka 90 länder. Vi levererar en innovativ, vetenskapsbaserad portfölj av premiumvarumärken och tjänster som täcker hela spektrumet av den snabbt växande dermatologimarknaden genom Injektionsestetik, Dermatologisk hudvård och Terapeutisk dermatologi.

Sedan vår grundades 1981 har vi med fokus och passion ägnat oss åt människokroppens största organ - huden - och möter individuella behov hos konsumenter och patienter genom överlägsna resultat i samarbete med hälso- och sjukvårdspersonal. Eftersom vi förstår att huden formar våra liv, driver vi dermatologin framåt för varje hudhistoria.

Jobbeskrivning

Som Maintenance Engineer ansvarar du för att underhålla och förbättra prestanda, tillförlitlighet och efterlevnad för vår produktionsutrustning och våra system. Du arbetar i nära samarbete med produktion, teknik, kvalitet och externa partners för att säkerställa att underhåll, kalibrering och inspektioner planeras och genomförs enligt interna standarder och regulatoriska krav.

Rollen kombinerar praktiskt tekniskt arbete med planering, koordinering, dokumentation och kontinuerliga förbättringar. Du förväntas arbeta självständigt, fatta välgrundade tekniska beslut inom ditt ansvarsområde och aktivt bidra till en säker och effektiv GMP-reglerad produktionsmiljö.

Huvudsakliga arbetsuppgifter

I denna roll tar du helhetsansvar för underhållsaktiviteter genom hela livscykeln - från planering till genomförande och uppföljning. Dina arbetsuppgifter omfattar både operativt arbete och förbättringsarbete. Du kommer bland annat att:

* Planera, koordinera och följa upp förebyggande och avhjälpande underhåll för att säkerställa hög tillgänglighet på utrustning och säker produktion
* Leda eller delta i större underhållsaktiviteter, produktionsstopp och tekniska projekt
* Säkerställa efterlevnad av GMP, interna rutiner och regulatoriska krav kopplade till underhåll och kalibrering
* Utveckla, uppdatera och förvalta styrande instruktioner, rutiner och systemdokumentation
* Ansvara för serviceavtal och samarbeta nära med externa leverantörer
* Driva och hantera avvikelser (NC) samt korrigerande åtgärder (CA/CC)
* Säkerställa korrekt reservdelstillgänglighet och effektiv underhållsplanering
* Arbeta i och ansvara för produktionsnära IT-system såsom CMMS
* Genomföra periodiska genomgångar av utrustning, system och dokumentation
* Aktivt bidra till initiativ för kontinuerliga förbättringar och ökad tillförlitlighet

Kvalifikationer och krav

För att lyckas i rollen ser vi att du har en stark teknisk grund kombinerad med ett strukturerat och kvalitetsdrivet arbetssätt. Du är bekväm med att ta ansvar, arbeta självständigt och samarbeta tvärfunktionellt. Vi söker dig som har:

* Kandidatexamen inom teknik (mekanik, el, automation, produktion eller liknande), eller motsvarande relevant erfarenhet
* 2-5 års erfarenhet av underhåll eller reparation och underhåll inom tillverknings- eller industrimiljö
* Erfarenhet av arbete i ett reglerat kvalitetssystem, gärna GMP
* Praktisk erfarenhet av industriell utrustning i produktionsmiljö
* Erfarenhet av planering, koordinering och genomförande av underhåll
* God förståelse för efterlevnad, dokumentation och regulatoriska krav
* Förmåga att fatta tekniska beslut inom ditt ansvarsområde
* Mycket god kommunikationsförmåga i både svenska och engelska

Varför Galderma i Uppsala?

Galdermas anläggning i Uppsala är vårt globala Center of Excellence för Estetik och hem för över 800 medarbetare inom FoU, tillverkning, klinisk utveckling och marknadsföring - allt under samma tak. Detta skapar en unik miljö där samarbetet är nära, kunskap delas och idéer snabbt blir verklighet.

Här blir du en del av ett tvärfunktionellt team där vetenskap möter tillämpning, och där ditt bidrag direkt påverkar produkter som används av patienter och konsumenter världen över.

Vad vi erbjuder

På Galderma erbjuder vi mer än bara en roll - vi erbjuder en miljö där du kan växa, utvecklas och göra verklig skillnad. Du blir en del av en global organisation med starka värderingar, modernt ledarskap och tydligt framtidsfokus. Hos oss kan du förvänta dig:

* Karriärutveckling och kontinuerliga lärandemöjligheter
* Attraktiva förmåner och bonusmodeller
* Innovativa och tekniskt utmanande projekt
* En global, inkluderande och samarbetsinriktad kultur
* Stark laganda och högt engagemang
* Fokus på balans mellan arbete och privatliv samt välmående Visa mindre

Help Shape the Future of Aesthetic Science

At Galderma, we are driven by one purpose - to advance dermatology for every skin story.
We are now looking for a passionate and hands-on Process Development Engineer to join our Assembly & Packaging team within Manufacturing Science and Technology (MSAT) in Uppsala.

In this role, you will play a key part in technology transfer, process validation, and continuous improvement activities for our world-leading biopharmaceutical and medical device manufacturing operations.

If you are ready to bring your engineering expertise into a global GMP environment where science meets innovation - this is your opportunity to make a real impact.



About the Role

As a Process Development Engineer, you will act as a subject matter expert (SME) for assembly and packaging processes within commercial manufacturing.
You will support new product introductions (NPI), drive tech transfer projects, and ensure robust and compliant manufacturing processes through validation, risk management, and investigation work.



Key responsibilities include:

* Lead and support technology transfer activities including comparability assessments and process performance qualification.
* Acting as a process owner for assembly and packaging, providing technical support to production.
* Lead investigations and problem-solving activities including root cause analyses, and corrective and preventive actions (CAPA).
* Supporting process validation, change control, and risk management activities.
* Review and contribute to GMP documentation, including SOPs, change controls, and qualification protocols
* Preparing and reviewing technical and validation documentation in line with GMP and regulatory requirements.
* Collaborating cross-functionally with Production, QA, RA, and R&D to ensure alignment, efficiency, and quality.
* Driving continuous improvement, cost-reduction initiatives, and operational excellence within manufacturing.



Are You the One We are Looking For?

You are a motivated engineer with a strong technical foundation and a passion for biopharma or medical device manufacturing.
You thrive in a GMP-regulated environment, take ownership of your work, and enjoy solving complex technical challenges in collaboration with others.

You bring curiosity, initiative, and structure - with the confidence to lead projects and the humility to work as part of a team.



Skills & Qualifications

Must-Haves (Knock-Out Criteria):

Degree: BSc or MSc in Life sciences, Engineering or related scientific discipline. Industry Experience: Minimum 3-5 years of hands-on experience in biopharmaceutical or medical device manufacturing within assembly and/or packaging. Tech Transfer: Proven experience transferring processes from development to commercial manufacturing or between GMP production sites. Investigation Skills: Solid experience in deviation handling, root cause analysis, and CAPA implementation; capable of performing technical and impact assessments in support of commercial operations. GMP Knowledge: Strong understanding of regulatory frameworks, cGMP compliance, and manufacturing documentation standards. Strong knowledge of EU/US GMP guidelines and regulatory standards. Strategic and analytical thinking with the ability to assess risks and make balanced decisions.



Strong Nice-to-Haves:

* Experience with Lean or Six Sigma methodologies.
* Background in process validation, protocol writing, and reporting.
* Exposure to cross-functional collaboration (QA, RA, Production, R&D).
* Strong documentation and analytical skills, including statistical process monitoring.
* Strong technical writing and communication skills.
* Familiarity with CPV (Continued Process Verification), FMEA, and risk assessments.



Why Join Galderma in Uppsala?

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to more than 800 professionals working across R&D, manufacturing, clinical development, and marketing - all under one roof.

You'll have the chance to work on innovative injectable and aesthetic products that combine biotechnology, medical device design, and advanced process engineering.





Ready to Make a Real-World Impact?

If you are ready to shape the next generation of aesthetic and biopharmaceutical manufacturing, apply today!

We review applications on a continuous basis, so please submit yours as soon as possible - the position may be filled before the closing date.

Bring your expertise. Shape the future. Join Galderma. Visa mindre

Job Title: Process Development Engineer, Biologics (Drug Substance or Drug Product)

Location: Uppsala, Sweden (Hybrid)



Job description :

We are looking for a new member to the Biologics team within Manufacturing Science and Technology. The Process Development Engineer is a subject matter expert (SME) responsible for new product implementation (NPI) into a manufacturing facility.



Key responsibilities:

*

Support new product implementation (NPI) strategy and all aspects of process validation, including process data reviews, investigations, risk management, and change implementation. Write validation documentation and execute process validation under guidance from senior scientists.
*

Serve as a technical SME representing MSAT in Technology Transfer projects.
*

Process owner to support day-to-day operations with a focus on continuous improvements. Identify opportunities for process enhancement, cost reduction, and efficiency gains, proactively driving necessary changes.
*

Lead and participate in investigations into deviations, incidents, and anomalies within the manufacturing process. Conduct in-depth root cause analysis to identify the underlying reasons for deviations and incidents, focusing on process improvement.
*

Collect data from various sources, including quality control reports, production logs, and other relevant documents, to support investigations and continuous process verification (CPV)
*

Write and review technical documentation ensuring compliance with regulatory and quality standards.
*

Coordinate with other experts and collaborate with cross-functional teams, including production, quality assurance, regulatory affairs, and process development, to ensure thorough investigation and timely issue resolution. Assist senior scientists in information gathering to support research studies and claims, and provide input to risk assessments/FMEAs.
*

Prepare detailed investigation reports, conveying findings and recommendations to management and relevant stakeholders



Skills & Qualifications

*

BSc or MSc in a relevant scientific or engineering field, such as Chemistry, Biochemistry, Chemical Engineering, or related discipline
*

Minimum of 2 years of experience in a biopharmaceutical environment
*

Familiarity with manufacturing processes in the biopharmaceutical industry
*

Experience in investigative methodologies and root cause analysis techniques





What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



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 600 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.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

We're now looking for a passionate and driven Automation Engineer to join our Operations Engineering team in Uppsala and play a key role in shaping the future of manufacturing automation at Galderma. If you thrive in a GMP-regulated environment, enjoy solving complex technical challenges, and want to make a real impact on production performance and reliability - this is your opportunity.

At Galderma, we're not just offering a job - we're inviting you to be part of something bigger. As a global leader in dermatology, we combine purpose with innovation to improve the lives of millions.



About Galderma:

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.



Job Description

As an Automation Engineer based in Uppsala, you will manage, plan, and oversee the implementation of engineering plans and programs related to operational automation systems and manufacturing lines. You will ensure that systems meet required safety, quality, compliance, and performance standards within a GMP-regulated environment.

In this role, you will develop and execute engineering plans, analyze trends and recurring issues in manufacturing automation systems, and provide robust, sustainable solutions that secure high system availability and optimized Overall Equipment Effectiveness (OEE). You will collaborate closely with cross-functional teams, represent Engineering in projects, and maintain strong relationships with internal stakeholders and external suppliers.

You will act as an individual contributor with recognized intermediate expertise in automation, working independently with moderate supervision while contributing to coordination across engineering and operational areas.

Key Responsibilities

In this position, you will play a central role in ensuring reliable and compliant automation systems that support our manufacturing operations. Your responsibilities include:

* Providing expert troubleshooting and maintenance support for existing automation systems, ensuring maximum uptime and system performance.
* Programming and configuring automation systems including PLCs, HMIs, SCADA platforms, and related control systems.
* Supporting the design and development of automation solutions for biopharmaceutical manufacturing processes.
* Collaborating with cross-functional teams to ensure alignment with site standards, project requirements, and engineering strategies.
* Implementing best practices to enhance system reliability, scalability, and Overall Equipment Efficiency (OEE).
* Creating automation-related change controls and executing Computer System Validation (CSV) activities in accordance with GMP and Part 11 requirements.
* Investigating automation-related deviations, supporting root cause analysis (RCA/RCCA), and implementing corrective and preventive actions.
* Performing automation computer system support activities such as system backups, performance monitoring, and user/password administration.
* Providing technical support for automation control platforms and process information systems (e.g., data historians).
* Contributing to capital project execution and supporting machinery/system design activities.
* Ensuring all work is executed in compliance with GMP, internal policies, procedures, safety rules, and regulatory standards, including participation in internal and regulatory audits.



Key Requirements & Qualifications

We are looking for a technically skilled and solution-oriented professional who combines analytical thinking with hands-on capability in automated production environments.

* Bachelor's degree in Electrical Engineering, Control Engineering, Electronic Engineering, or equivalent experience.
* Minimum of 3 years' experience configuring and supporting automation systems, including PLCs, HMIs, and SCADA solutions.
* Experience working in a GMP-regulated environment and familiarity with Part 11 requirements, or experience from a similarly regulated industry.
* Experience with SCADA systems and related platforms such as Siemens, WinCC, iFix, Wonderware, and data historians.
* Experience in capital project execution and/or machinery or system design is considered an advantage.
* Professional level of English; Swedish is desirable.
* Solid understanding of project management processes and structured problem-solving methodologies.



Why Join Galderma in Uppsala?

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics - home to over 800 professionals working across R&D, manufacturing, clinical development, and marketing, all under one roof. You'll be part of a multidisciplinary team where science meets application.



About Galderma:
Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story. Visa mindre

We're now looking for a passionate and driven MS&T Scientist - Cleaning Validation to join our team and ensure world-class contamination control and compliance in pharmaceutical manufacturing.
If you're ready to bring science to life and make an impact beyond the lab - this is your chance.

At [Company Name], we're not just offering a job - we're inviting you to be part of something bigger. As a global leader in healthcare innovation, we combine purpose with technology to improve the lives of millions.



About Galderma:

Galderma is a global leader in pharmaceutical and biopharmaceutical solutions, present in over 90 countries. We deliver innovative, science-based products and services that meet the highest standards of quality and safety. Since our foundation, we have dedicated our focus and passion to advancing healthcare and improving patient outcomes worldwide.



Job Description

As an MS&T Scientist - Cleaning Validation, you will provide technical expertise and operational support for cleaning validation activities across pharmaceutical manufacturing processes. Your role ensures that equipment cleaning procedures are scientifically justified, compliant with global regulatory standards, and effective in preventing cross-contamination. You will collaborate with MS&T process owners, QA, and Production to deliver robust validation strategies and maintain inspection readiness.



Key Responsibilities

* Develop and validate cleaning processes (manual, CIP/SIP) and analytical methods (TOC, HPLC, LC-MS).
* Author and execute cleaning validation protocols and reports.
* Perform risk assessments and establish acceptance criteria based on regulatory guidance.
* Ensure compliance with GMP, FDA, EMA, ICH, and PIC/S guidelines.
* Support regulatory submissions and health authority inspections.
* Collaborate cross-functionally with Development, Production, QA, QC, and Engineering.
* Drive continuous improvement initiatives to optimize cleaning procedures and reduce downtime.



Key Requirements & Qualifications

* MSc/PhD in Pharmaceutical Sciences, Chemistry, Biotechnology, or related field.
* 3-5 years of experience in pharmaceutical manufacturing or validation, with a focus on cleaning validation.
* Strong knowledge of GMP and cleaning validation principles.
* Excellent problem-solving, documentation, and communication skills.
* Ability to work independently and in cross-functional teams.
* Hands-on experience with injectable manufacturing processes is a plus.
* Lean or Six Sigma certification preferred.



Why Join Us?

Our site in Uppsala is a global center of excellence - home to hundreds of professionals working across R&D, manufacturing, and quality, all under one roof. You'll be part of a multidisciplinary team where science meets application.

What we offer:

* Career development & learning opportunities
* Attractive benefits and bonus models
* Innovative projects
* Global & inclusive culture
* Strong team spirit & engagement
* Work-life balance & wellbeing



Are You the One We're Looking For?

We look for people who focus on results, embrace learning, and bring positive energy. We combine initiative with teamwork and collaboration. Above all, we are passionate about doing something meaningful for patients and healthcare professionals.

With us, you have the ultimate opportunity to gain new and challenging work experience and create an unparalleled, direct impact.

Please add the content of the job posting here. It will be used to attract the best candidates so make sure to include the mission, responsibilities and requirements of the role. Visa mindre

Electrician
Location: Uppsala, Sweden (on-site)



Jobb beskrivning

Arbeta som Elektriker på Galderma i Uppsala!

Galderma är i en mycket expansiv och spännande fas, vi har bland annat byggt en helt ny fabrik på vårt område. Nu söker vi en elektriker till vår serviceorganisation. Rollen är operativ och innebär varierande eluppdrag över hela anläggningen, från felsökning och underhåll till installationer och driftstöd.

Du arbetar nära vår elsäkerhetsansvarig och blir en viktig del i att hålla produktionen i gång.

Det betyder att arbeten ibland måste planeras utifrån produktionsbehov, vilket ibland kan innebära utmaningar när det gäller planeringen, att hitta servicefönster och liknande.



Vissa uppdrag kan ibland ske i klassade lokaler eller renrum vilket kräver extra noggrann planering och med rätta tillstånd. Men de flesta arbeten sker i vanliga produktions- och kontorslokaler. Tjänsten är en dagtidstjänst.

Hos oss blir du en del av ett team med stark sammanhållning, humor och mycket skratt. Du får arbeta i en miljö med högt kvalitets- och säkerhetsfokus och goda möjligheter till utveckling inom el, energioptimering och analys samt inom produktionstekniska områden.

Vi söker dig som är kommunikativ, lyhörd och serviceinriktad, och med hög social kompetens. Du är självgående, strukturerad och kan planera och prioritera ditt arbete självständigt, samtidigt som du samarbetar nära kollegor och elsäkerhetsansvarig. Noggrannhet och kvalitetsfokus är en självklarhet, inklusive att dokumentera utförda arbeten. Teamet är litet, därför kräver rollen stor anpassningsförmåga och flexibilitet och du får räkna med att supportera verksamheten inom många olika områden.



Ansvarsområden

* Utföra varierande elarbeten över hela Galdermas site i Uppsala, inklusive installation, underhåll och felsökning.
* Samverka nära elsäkerhetsansvarig för rådgivning och stöd i elfrågor.
* Arbeta med förebyggande elarbeten för att upprätthålla hög elsäkerhetsnivå.
* Utföra besiktningar och periodiska kontroller.
* Bidra till problemlösning och service på ett proaktivt och flexibelt sätt, där produktionens behov alltid prioriteras.



Kvalifikationer

* Några års erfarenhet av elektriska installationer, gärna inom industriell miljö
* Behörig elektriker (ECY-certifikat)
* B-körkort
* Svenska och grundläggande engelska i tal och skrift

Meriterande

* Praktisk erfarenhet från industriell tillverkning eller liknande produktionsmiljö



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.

Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss i moderna lokaler utmed vackra Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag, dock senast den 20 februari 2026. Urval och intervjuer görs löpande under ansökningstiden och tjänsten kan komma att tillsättas innan sista ansökningsdatum.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal digitalt med rekryteraren
* Nästa steg är en intervju med anställande chef samt elsäkerhetsansvarig på plats
* Slutligen genomförs en säkerhetsprövningsintervju via vår externa leverantör samt referenstagning innan ett eventuellt erbjudande lämnas



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Location: Uppsala

Employment type: Full-time

Galderma växer och står inför en spännande resa och nu söker vi en erfaren QC Analyst till vår grupp Bioassay inom Quality Control! Är du en driven och engagerad analytiker med intresse för att arbeta i laboratoriemiljö och samtidigt bidra till att bygga framtidens QC verksamhet inom Galderma? Då är detta rollen för dig!
Som QC Analyst inom QC Bioassay blir du en nyckelperson i vårt laboratorium. Här kommer du arbeta med cellbaserad potensanalys och tillsammans med dina kollegor ta hand om labb, utrustning och metoder. Du kommer att arbeta med cellodlingar, Western Blot och statistiska analysmetoder. Som QC Analyst kommer du, utöver analysuppdraget, även att arbeta aktivt med förbättringsarbete med fokus på att effektivisera gemensamma processer.

Ansvarsområden

* Utföra och dokumentera potensanalyser enligt instruktioner
* Granska analytiska resultat
* Ansvara för instrument, och analysmetoder
* Kvalificering av utrustning
* Skapa och uppdatera interna instruktioner och dokument
* Att arbeta enligt GMP
* Bidra till en positiv och kollaborativ arbetsmiljö
* Bidra till att effektivisera QCs arbetssätt och processer

Kvalifikationer

* Naturvetenskaplig högskoleutbildning motsvarande minst kandidatexamen.
* Flera års erfarenheter inom laborativ verksamhet, meriterande är erfarenhet av cellodling, proteinanalyser, western blot och/eller antikroppsarbete
* Erfarenhet att jobba i GMP-miljö är meriterande
* Flytande svenska i tal och skrift
* Erfarenhet av förbättringsarbete är önskvärt



Vi söker dig som har mod att utmana kända processer, som tar initiativ till förbättringar och som vill bidra till en mer effektiv kvalitetskontroll. Du är lätt att samarbeta med, har en stark teamkänsla och kundfokus samt ett noggrant och kvalitetsmedvetet arbetssätt. Hos oss värdesätter vi personer som vågar ta ansvar. Med ditt driv och självledarskap blir du snabbt självgående och kan planera och prioritera arbetet så att resultaten märks.



Vi erbjuder
Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.
I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.
På Galderma i Uppsala har vi verksamhet inom produktutveckling och tillverkning inom dermatologi och vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Vi är belägna längs med Fyrisån i Uppsala, 10 minuters cykelfärd från Uppsala Resecentrum. Visa mindre

Junior Process Engineer/Projektoperatör

Job title: Junior Process Engineer/Projektoperatör

Location: Uppsala, Sweden (Onsite)



På Galdermas Uppsalasite pågår driftsättandet av vår nya fabrik för fullt. Det är en fabrik med hög automationsgrad, den senaste tekniken och digitalisering. I denna fabrik söker vi nu fler medarbetare som kan bidra med sin kunskap och framåtanda för att skapa så optimerade och välfungerande processer och arbetssätt som möjligt.



Om rollen

Vi söker en engagerad och utvecklingsorienterad Junior Process Engineer/Projektoperatör för möjligheten att vara med och påverka och forma sin arbetslinje och processerna från grunden i vår framtidsfabrik och verksamheten man sen kommer att arbeta i.

Här får man chansen att bygga nyttig kunskap och bli en expert på sin utrustning inför att det är dags för reguljär produktion.

Rollen är en anställning som Projektoperatör i grunden med en tillsvidareanställning och lönetillägg som Junior Process Engineer som löper under den tid projektet pågår. När projektet fasas ut övergår anställningen i en roll som Processoperatör.



Rollen är i en nystartad gruppering för produktionsprocesserna formulering, aseptisk vialfyllning och avsyning i projektet med driftsättande av vår nybyggda fabrik och nya produktionslinor. Gruppen består idag utav 5 Junior Process Engineers där vardera medarbetare har primärt fokus på ett av dom tre arbetsområdena formulering, fyllning eller avsyning.

Du kommer vara delaktig i att bygga instruktioner och processer från grunden och vara med och sätta din prägel på vår framtida fabrik.

Arbetet är till en början i oklassad miljö men vid reguljär produktion råder renrumsklass C och D.



Huvudsakliga arbetsuppgifter

* Vara med vid installation och kvalificering av nya utrustningar.
* Framtagande av ny dokumentation och handhavandet av processerna med fokus på att tänka nytt och förbättra befintliga arbetssätt.
* Vara delaktig i och forma arbetet kring arbetsmiljö och säkra processer.
* Framtagande av digitala batchprotokoll och arbete med MES-systemet PAS-X.
* När projektet fasas ut kommer du att vara en av dem första i arbetsgruppen som utbildar och bygger upp kommande skiftlag och gör dig och din arbetsgrupp redo för kommersiell tillverkning.



Vem söker vi:

* Erfaren inom operatörsarbete i renrumsmiljö.
* Tidigare erfarenhet av att arbeta i projekt.
* Kvalitetsmedveten och kunnig inom GMP och EudraLex volym 4.
* Goda kunskaper i word och excel.
* Van att planera och prioritera ditt arbete för att möta förväntade leveranser och deadlines.
* Erfarenhet av att utbilda praktiskt och teoretiskt inom produktionsprocesser.
* Goda kunskaper i svenska och engelska både i tal och skrift.



Meriterande:

* Tidigare aseptisk kompetens.
* Kunskap i PAS-X.
* Rollen vi söker är med primärt fokus mot processer i C-klass. Tidigare erfarenhet kring arbete i C-klass är meriterande.



Vi ser gärna att du är en kommunikativ och initiativtagande person som jobbar bra både självständigt och i grupp och som tar stort ägandeskap för sitt arbete.



Varför komma till oss?

Ta den unika chansen att vara med och bygga en fabrik och dess processer från grunden. Var med och bestäm hur processerna ska se ut där du i framtiden kommer att arbeta.



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.

Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss i moderna lokaler utmed vackra Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag, dock senast den 29 januari 2025. Urval och intervjuer görs löpande under ansökningstiden, tjänsten kan komma att tillsättas innan sista ansökningsdatum.

Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren



Nästa steg är en intervju med anställande chef + eventuell chefskollega på plats hos Galderma

Slutligen genomförs en säkerhetsprövning via vår externa leverantör samt referenstagning innan ett eventuellt erbjudande lämnas



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Help Shape the Future of Aesthetic Science

At Galderma, we are driven by one purpose - to advance dermatology for every skin story.
We are now looking for a passionate and hands-on Process Development Engineer to join our Assembly & Packaging team within Manufacturing Science and Technology (MSAT) in Uppsala.

In this role, you will play a key part in technology transfer, process validation, and continuous improvement activities for our world-leading biopharmaceutical and medical device manufacturing operations.

If you are ready to bring your engineering expertise into a global GMP environment where science meets innovation - this is your opportunity to make a real impact.



About the Role

As a Process Development Engineer, you will act as a subject matter expert (SME) for assembly and packaging processes within commercial manufacturing.
You will support new product introductions (NPI), drive tech transfer projects, and ensure robust and compliant manufacturing processes through validation, risk management, and investigation work.



Key responsibilities include:

* Lead and support technology transfer activities including comparability assessments and process performance qualification.
* Acting as a process owner for assembly and packaging, providing technical support to production.
* Lead investigations and problem-solving activities including root cause analyses, and corrective and preventive actions (CAPA).
* Supporting process validation, change control, and risk management activities.
* Review and contribute to GMP documentation, including SOPs, change controls, and qualification protocols
* Preparing and reviewing technical and validation documentation in line with GMP and regulatory requirements.
* Collaborating cross-functionally with Production, QA, RA, and R&D to ensure alignment, efficiency, and quality.
* Driving continuous improvement, cost-reduction initiatives, and operational excellence within manufacturing.



Are You the One We are Looking For?

You are a motivated engineer with a strong technical foundation and a passion for biopharma or medical device manufacturing.
You thrive in a GMP-regulated environment, take ownership of your work, and enjoy solving complex technical challenges in collaboration with others.

You bring curiosity, initiative, and structure - with the confidence to lead projects and the humility to work as part of a team.



Skills & Qualifications

Must-Haves (Knock-Out Criteria):

Degree: BSc or MSc in Life sciences, Engineering or related scientific discipline. Industry Experience: Minimum 3-5 years of hands-on experience in biopharmaceutical or medical device manufacturing within assembly and/or packaging. Tech Transfer: Proven experience transferring processes from development to commercial manufacturing or between GMP production sites. Investigation Skills: Solid experience in deviation handling, root cause analysis, and CAPA implementation; capable of performing technical and impact assessments in support of commercial operations. GMP Knowledge: Strong understanding of regulatory frameworks, cGMP compliance, and manufacturing documentation standards. Strong knowledge of EU/US GMP guidelines and regulatory standards. Strategic and analytical thinking with the ability to assess risks and make balanced decisions.



Strong Nice-to-Haves:

* Experience with Lean or Six Sigma methodologies.
* Background in process validation, protocol writing, and reporting.
* Exposure to cross-functional collaboration (QA, RA, Production, R&D).
* Strong documentation and analytical skills, including statistical process monitoring.
* Strong technical writing and communication skills.
* Familiarity with CPV (Continued Process Verification), FMEA, and risk assessments.



Why Join Galderma in Uppsala?

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to more than 800 professionals working across R&D, manufacturing, clinical development, and marketing - all under one roof.

You'll have the chance to work on innovative injectable and aesthetic products that combine biotechnology, medical device design, and advanced process engineering.





Ready to Make a Real-World Impact?

If you are ready to shape the next generation of aesthetic and biopharmaceutical manufacturing, apply today!

We review applications on a continuous basis, so please submit yours as soon as possible - the position may be filled before the closing date.

Bring your expertise. Shape the future. Join Galderma. Visa mindre

Job Title: Manager MSAT Device Injectables

Location: Uppsala, Sweden (Hybrid)



We are looking for a passionate and strategic Manager Devices and Injectables to join our world-class MS&T organization in Uppsala. This is a unique opportunity to lead the technical strategy, process excellence, and lifecycle management for Galderma's most advanced injectable and device products - shaping global launches, driving innovation, and ensuring manufacturing performance that impacts millions of patients worldwide.

At Galderma, you won't just take on a job - you'll contribute to science-driven solutions, guide a high-performing team, and build the next generation of manufacturing capability. If you're ready to combine leadership with meaningful impact, this is the role for you.



About Galderma

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of flagship brands and services across Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology.

Since 1981, we have dedicated our focus and passion to the human body's largest organ - the skin. By understanding that the skin we are in shapes our lives, we are advancing dermatology for every skin story.



Job Description

As Manager Devices and Injectables, you will lead the technical lifecycle management of Devices and Injectables and act as a key driver for robust manufacturing processes. You will serve as a technical authority, ensure compliance with global regulatory expectations, and lead a team of MS&T specialists dedicated to injectable and device manufacturing.

Your focus will span process validation, tech transfer, CPV, troubleshooting, investigations, and continuous improvement - forming the backbone of safe, high-quality, and efficient production.



Key Responsibilities

As the Manager Devices and Injectables, you will drive technical strategy and operational excellence across manufacturing processes. Acting as a technical authority, you will ensure products are manufactured safely, efficiently, and in full compliance with global standards.

You will lead and support new product introductions, major technology transfer activities, and product remediation initiatives, while ensuring process knowledge is maintained and continuously improved. A core part of your role is to assess the impact of manufacturing changes, define and track technical CAPAs, and provide MS&T expertise during deviations, investigations, and technical complaints.

You will develop and execute process validation and revalidation strategies, author and review protocols and reports, and oversee ongoing continued process verification and annual product reviews. Your analyses will feed into recommendations for corrective actions and long-term improvements.

Collaboration is central: you will work closely with Production, Quality, Engineering, R&D, and global partners to resolve shop-floor challenges, support change controls, lead risk assessments, and provide technical insight during supplier evaluations.

As a people leader, you will mentor and develop MS&T scientists, fostering an inclusive, collaborative environment where expertise grows and accountability thrives. You ensure operational continuity by delegating effectively and building a resilient, high-performing team.



Key Requirements & Qualifications

To succeed in this role, you bring a strong mix of technical depth, leadership capability, and regulatory understanding within pharmaceutical and medical device manufacturing, particularly in Devices and Injectables. You are comfortable navigating a global environment and balancing strategic decision-making with hands-on technical support.

You likely have 10+ years of experience in pharma or medical device manufacturing, ideally with exposure to Devices and Injectables, fill-finish, or related processes, and at least 3 years of managerial experience, guiding technical experts or cross-functional teams.

Your background includes a solid foundation in manufacturing science and technology, experience in technology transfer, and a strong track record in process validation (PPQ, CPV) and lifecycle management. You are well-versed in GMP, ISO 13485, ICH, and global regulatory expectations, and have led investigations, performed root-cause analyses, implemented CAPAs, and contributed to regulatory submissions (IND, BLA, NDA, or variations).

Core competencies include:

* Leading technology transfers from development to commercial manufacturing
* Designing, executing, and reviewing process validation and revalidation protocols
* Managing deviation investigations and implementing CAPAs
* Supporting regulatory submissions and compliance inspections
* Collaborating across matrix and international teams

Strong communication skills, the ability to explain complex technical topics to diverse stakeholders, and fluency in English are essential.

Additional strengths that are highly beneficial include experience with structured problem-solving tools (FMEA, Ishikawa, 5 Whys), global or cross-border technology transfers, project management certifications (PMP, PRINCE2), and Swedish language skills.



Why Join Galderma in Uppsala?

Our Uppsala site is Galderma's Global Center of Excellence for Aesthetics - home to over 800 professionals across R&D, manufacturing, engineering, and clinical development. Here, science meets real-world application and innovation becomes product reality.

What we offer

* Career development & learning opportunities
* Attractive benefits and bonus programs
* High-impact Devices and Injectables projects
* A global & inclusive culture
* Strong team spirit and engagement
* Work-life balance & wellbeing initiatives



Are You the One We're Looking For?

We seek people who take ownership, drive results, embrace learning, and bring positive energy to their teams. You combine initiative with collaboration and are motivated by contributing to something that truly matters for patients, consumers, and healthcare professionals.

At Galderma, we empower employees, develop strengths, and celebrate diversity. Here, you will grow your career, expand your expertise, and make a meaningful difference. Visa mindre

Aseptik Operatör (Aseptisk fyllning)

Location: Uppsala (on-site, skiftgång)



Job Description

Nu har du möjlighet att bli en del av Galdermas tillväxtresa och utvecklas i rollen som aseptik operatör!

Vi söker nu en ny operatör till vår läkemedelstillverkning där du har möjligheten att vara med i tillverkningen av vår läkemedelsprodukt Relfydess. I tjänsten ingår formulering och aseptisk fyllning av Relfydess.

Nuvarande produktionsgrupp på lina 4 består idag av operatörer, labingenjörer samt process- och kvalitetsingenjörer. Tillsammans är ni ansvariga för tillverkning, förvaltning och utveckling av produktionsprocesser för vår biologiska läkemedelsprodukt. Gruppen har en mycket god gemenskap och värdesätter ett arbetsklimat där alla ska trivas.



Ansvarsområden

Rollen är riktad mot den del av linan som ansvarar för formulering (bulk) och aseptisk fyllning.

I tjänsten kommer du att:

* Delta aktivt och ta ansvarar för att tillverkning utförs enligt uppsatta instruktioner och specificerade kvalitetskrav.
* Delta i den dagliga tillverkningsprocessen samt mediafyllningar
* Ta ansvar för processer och utrustning inom ditt ansvarsområde
* Dela med dig av din kunskap till andra för att med stort kundfokus leverera en kvalitetssäkrad produkt till marknaden.



Kvalifikationer:

* Erfarenhet av aseptiskt operatörsarbete (meriterande)
* Kunskap om och erfarenhet av att arbeta med strikt aseptiska processer inom läkemedelsproduktion.
* Förmåga att följa och dokumentera strikt efterlevnad av GMP.
* Avslutad gymnasieutbildning.
* Flytande svenska, både i tal och skrift



Som operatör inom läkemedelsbranschen är det viktigt att du är noggrann och har ett kvalitetstänk, samt att du har god samarbetsförmåga. Du är behjälplig och kan integrera med teamet där ge och ta feedback är en viktig del i det dagliga arbetet. Rollen kräver att du är driven och lugn, samt tar ansvar för ditt arbete. Du är flexibel och uppskattar den höga pulsen produktionen, samtidigt som du trivs bra med rutinarbete.



Övrigt

Tjänsten innebär skiftarbete. För närvarande tillämpas 3-skift inklusive helgarbete.



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.

Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss i moderna lokaler utmed vackra Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag. Urval och intervjuer görs löpande under ansökningstiden och tjänsten kan komma att tillsättas innan sista ansökningsdatum, 17 februari 2026.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren
* Nästa steg är en intervju på plats med anställande chef + operatör från teamet
* Sista steget är en säkerhetsklassning samt referenstagning



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Job Title: Senior Sterilization Process Development Scientist/Engineer

Location: Uppsala, Sweden, On-site



Job Description

Are you an experienced aseptic processing professional with experience in the sterilization of pharmaceuticals or medical devices? If so, this could be the role for you as we are now hiring a Senior Scientist/Engineer in our Injectable Development team.

Elevate your career by joining Galderma for a role that involves subject-matter expertise in the field of sterilization process development and process transfer to manufacturing facilities for both injectable medical devices and pharmaceuticals. As an integral part of the Product Science department, you will be highly involved in developing new products to further expand Galderma's portfolio and building our parenteral technology capabilities.



Key responsibilities

* Act as a steam sterilization Subject Matter Expert (SME) for projects and provide required experimental designs, data and author technical reports compliant with regulatory guidelines and industrial standards.
* Lead activities related to sterilization process development of injectable products under development, including work with regulatory submissions, design control, specifications, and risk assessments.
* Represent the Process Science team in cross functional product development teams with other internal departments and external manufacturing partners.
* Participate in key Product Science activities to assess impact of new regulations and implement appropriate changes
* Keep up to date with innovations in aseptic and low bioburden processing, share and implement new technology in the organization.



Skills & Qualifications

* Expertise in development and validation of Steam-In-Place and terminal sterilization for parenteral products using steam/moist heat
* Experience with sterilization using irradiation methods is also desirable
* Strong knowledge in microbiological controls and the use of biological indicators including risk assessment, validation and environmental monitoring techniques
* Knowledge of cGMP and Design Control in regulatory controlled work environments (e.g. ISO 13485, 21 CFR820, ICHQ8, 21CFR210/211, etc.) and experience preparing regulatory filings and supporting documentation
* Fluent in English, ability to work in Swedish is also desirable.
* Strong communication skills, providing guidance and information to internal and external stakeholders and talking with regulatory bodies during inspections
* University degree in Chemical or Mechanical Engineering, Chemistry, Biochemistry, Biotechnology or similar technical field and 8 years experience in the pharmaceutical or medical device field.



What We Offer

At Galderma, we believe that our people are our most valuable asset and we are committed to creating an environment where you can thrive both professionally and personally.

When you join us, you can expect:

Competitive Compensation & Career Growth: Attractive salary and benefits, continuous learning and clear opportunities for advancement. Work on innovative projects that make a real difference in people's lives.

Global & Inclusive Culture: Collaborate across sites in North America, South America, and Europe in a diverse and inclusive environment that values teamwork and different perspectives.

Work-Life Balance & Wellbeing: Flexible working hours, wellness initiatives and on-site amenities including a fully equipped gym in a beautiful location by the river Fyris, just 10 minutes by bike from Uppsala city center.

Social Engagement & Team Spirit: Participate in an active leisure and sports club, enjoy quarterly town halls with fika, employee-led summer parties and celebrate key milestones such as Yellow Belt certifications together.



Next Steps

We welcome your application via our company website CAREERS | Galderma. Please apply as soon as possible as the selection process is ongoing and applications will be reviewed continuously.

If your profile matches our requirements, you will be invited to an initial virtual call with the recruiter.

The next step will be an interview with the hiring manager.

Then follows a panel discussion with the extended team.

Finally, a reference check is carried out before a possible offer is made.



We wish to inform applicants 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. Visa mindre

Underhållstekniker - tvåskift
Location: Uppsala, Sweden (on-site)



Arbetsbeskrivning
Vi söker en underhållstekniker för att stödja och förbättra vår verksamhet inom Engineering. Du kommer att vara involverad i att implementera planer, förbättra processer och samarbeta i innovativa projekt som driver vår verksamhet framåt.



Ansvarsområden

* Implementera tekniska planer och program för att stödja operativa aktiviteter inom olika tekniska funktioner.
* Spåra och anpassa aktiviteter för att förbättra processer, modifiera befintliga system och utveckla effektiva testprocedurer.
* Utföra tekniska processer och policyer, med fokus på utveckling av nya produkter och förbättring av befintliga.
* Analysera tekniktrender och säkerställ framgångsrik implementering av tekniska planer samtidigt som du följer kvalitets-, kostnads- och säkerhetsstandarder.
* Samarbeta för att bedöma teknisk genomförbarhet, kostnadseffektivitet och kundernas efterfrågan på produkter och processer.
* Delta i fälttester av produkter, processer och system för att säkerställa tillförlitlighet och prestanda.
* Underhåll och förbättra utrustning genom att felsöka problem, utföra förebyggande underhåll och säkerställa drifteffektivitet.



Kvalifikationer

* Högskoleutbildning inom relevant område eller motsvarande erfarenhet/behörighet.
* Viss erfarenhet inom praktiska ingenjörsuppgifter. Det är en fördel om du har erfarenhet inom styr- och regler, och/eller el.
* Flytande svenska och engelska.
* B-körkort.
* Stark analytisk och problemlösningsförmåga med känsla för detaljer.
* Förmåga att samarbeta effektivt med kollegor och bidra till tvärfunktionella team.
* Kännedom om tekniska standarder, säkerhetsprotokoll och kvalitetssäkring.
* Nyfiken på att lära sig och anpassa sig till ny teknik och tekniska trender.



Övrig information

Skiftgång förekommer i tjänsten. Arbetstiderna är förlagda till dag- och eftermiddagsskift. Dagtid arbetar du måndag till torsdag kl. 06:30-15:00 samt fredag kl. 06:30-17:10. Eftermiddagsskiftet gäller måndag till torsdag kl. 14:30-23:10, med lediga fredagar.



Vi erbjuder
Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.



På Galderma i Uppsala har vi verksamhet inom produktutveckling och tillverkning inom dermatologi och vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Vi är belägna längs med Fyrisån i Uppsala, 10 minuters cykelfärd från Uppsala Resecentrum.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag. Urval och intervjuer görs löpande under ansökningstiden och tjänsten kan komma att tillsättas före sista ansökningsdag, den 13 februari 2026.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren.
* Nästa steg är en intervju med anställande chef
* Sista steget är en panelintervju med teamet



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Job Title: Head of Innovation, Injectable Aesthetics

Location: Uppsala



About the role:

As the Head of Innovation, Injectable Aesthetics you will lead and shape the strategic direction of our Injectable Aesthetics Technical Innovation organization, driving alignment with the Global R&D strategy. This role requires a seasoned professional with proven leadership experience in highly matrixed environments and deep technical expertise in medical devices. You will spearhead early-stage exploration and development of cutting-edge injectable aesthetic solutions-including neuromodulators, dermal fillers, and biostimulators-while ensuring compliance with our quality systems, international standards, and regulatory requirements. By adapting and implementing strategies with both short- and long-term impact (1-5 years), you will play a pivotal role in advancing innovation and delivering results aligned with global and functional objectives.



Key Responsibilities:

* Translate business strategy and scientific trend exploration into effective Injectable Aesthetic innovation plans.
* Lead the Injectable Aesthetic technical innovations strategy, including projects and activities from early exploratory work to Target Product Profile finalization through transfer of oversight to cross-functional project core team.
* Build a strong and effective team of Product Research Leaders and direct them towards achievement of set objectives and communication with other department personnel.
* Responsible to leading and planning ways to optimize the entity or function including the team structure required to deliver results.
* Define and implement new ways of working, including new processes, with the Product Science organization.
* Act as a liaison and build potential relationships with critical stakeholders within and outside Galderma.
* Support external scientific collaborations and technical evaluations of Business Development opportunities as needed.
* Ensure support to Global Marketing teams with key technical expertise (e.g., congresses, GAIN events)
* Lead and manage the budget of the Injectable Aesthetic Technical Innovation team activities.
* Represent Global R&D in Uppsala Site Leadership team and develop strong, trusting cross-functional relationships with senior business leaders.





Skills & Qualifications:

* Master's degree or PhD in a relevant scientific or engineering discipline (e.g., Biomedical Engineering, Pharmaceutical Sciences, Medical Devices) or equivalent experience.
* Fluent in English and Swedish (both written and spoken).
* Proven track record of leading technical innovation teams in a highly matrixed, global organization.
* Deep knowledge of medical devices and injectable aesthetics (neuromodulators, dermal fillers, biostimulators), including regulatory and quality system requirements.
* Ability to translate business strategy and scientific trends into actionable innovation plans with short- and long-term impact.
* Strong capability to influence and build relationships across senior leadership and external partners.
* Experience in defining and implementing new processes and ways of working to optimize R&D functions.
* Demonstrated ability to manage budgets and allocate resources effectively.



We offer
You will work for an organization that embraces diversity and inclusion, and we believe that we deliver better results by reflecting the perspectives of our diverse customer base.

In Uppsala, Galderma's global center for the aesthetics business area is located, with operations in product development, manufacturing, and marketing. Approximately 600 people work here with world-leading products such as Restylane, Azzalure, and Sculptra.



We offer you the opportunity to work in an exciting, international environment where both personal and professional development are encouraged. With us, you will become an important part of a global and growing company. You will find us in modern premises along the beautiful Fyris River, only a 10-minute bike ride from Uppsala Central Station.



Next steps
Have we caught your interest? We welcome your application via the "Apply Now" link today, but no later than January 23, 2026. Selection and interviews are conducted on an ongoing basis during the application period and the position may be filled before the final application deadline.



Our people make a difference
At Galderma, you'll work with people who are like you-and people who are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos create the perfect environment for people to thrive and excel in what they do. Visa mindre

Operatör (Natt) (Aseptisk fyllning)

Location: Uppsala (on-site, natt, Mån-Tors 22.15-07:05)



Job Description

Nu har du möjlighet att bli en del av Galdermas tillväxtresa och utvecklas i rollen operatör!

Vi söker nu en ny operatör till vår läkemedelstillverkning där du har möjligheten att vara med från början i uppstarten av en ny produktionslina för vår framtida läkemedelsprodukt.

Nuvarande produktionsgrupp på lina 4 består idag av operatörer, labingenjörer samt process- och kvalitetsingenjörer. Tillsammans är ni ansvariga för tillverkning, förvaltning och utveckling av produktionsprocesser för vår biologiska läkemedelsprodukt. Gruppen har en mycket god gemenskap och värdesätter ett arbetsklimat där alla ska trivas. Denna tjänst innebär ständigt nattarbete men dagtid till en början som återgår till nattarbete efter genomförd några utbildningar.



Ansvarsområden

Rollen är riktad mot den del av linan som ansvarar för formulering (bulk) och aseptisk fyllning. I din tjänst kommer du att:

* Delta aktivt och ta ansvarar för att tillverkning utförs enligt uppsatta instruktioner och specificerade kvalitetskrav.
* Delta i den dagliga tillverkningsprocessen samt mediafyllningar
* Ta ansvar för processer och utrustning inom ditt ansvarsområde
* Delar med dig av din kunskap till andra för att med stort kundfokus leverera en kvalitetssäkrad produkt till marknaden.



Kvalifikationer:

* Avslutad gymnasieutbildning.
* Flytande svenska, både i tal och skrift.
* Förmåga att följa och dokumentera strikt efterlevnad av GMP.



Fördel om du har:

* Erfarenhet av aseptiskt operatörsarbete
* Kunskap om och erfarenhet av att arbeta med strikt aseptiska processer inom läkemedelsproduktion.
* Deltagande i mediafyllningar



Som operatör inom läkemedelsbranschen är det viktigt att du är noggrann och har ett kvalitetstänk, samt att du har god samarbetsförmåga. Du är behjälplig och kan integrera med teamet där ge och ta feedback är en viktig del i det dagliga arbetet. Rollen kräver att du är driven och lugn, samt tar ansvar för ditt arbete. Du är flexibel och uppskattar den höga pulsen produktionen, samtidigt som du trivs bra med rutinarbete.



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.



Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss i moderna lokaler utmed vackra Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag, dock senast 5 januari 2026. Urval och intervjuer görs löpande under ansökningstiden och tjänsten kan komma att tillsättas innan sista ansökningsdatum.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren.
* Nästa steg är en intervju med anställande chef + teamledare
* Sista steget är en säkerhetsklassning samt referenstagning



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Preclinical Principal Scientist - Injectable Medical Devices

???? Uppsala, Sweden | Hybrid | Full-time | Permanent

Shape the future of aesthetic innovation at Galderma

At Galderma, we're not just offering a job - we're inviting you to shape the future of dermatology. As a global leader in the science of skin, we combine purpose with innovation to improve the lives of millions.

Now, we're looking for a passionate and driven Preclinical Principal Scientist to join our team in Uppsala and lead the preclinical safety strategy for our next-generation injectable medical devices. If you're ready to bring science to life and make an impact beyond the lab, this is your chance.



Why join Galderma in Uppsala?

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 600 professionals working across R&D, manufacturing, clinical development, and marketing - all under one roof.

You'll be part of a multidisciplinary team where science meets application, with world-leading brands such as Restylane®, Azzalure®, and Sculptra®. We offer:

* A hybrid work model with flexible hours
* Continuous learning & career development opportunities
* A diverse, inclusive, and collaborative culture
* A modern workplace just 10 minutes from Uppsala Central Station



About the role

As Preclinical Principal Scientist, you'll be a key scientific leader responsible for defining and driving preclinical strategies for our injectable devices - from biocompatibility and toxicological risk assessments to supporting regulatory submissions and clinical trials.

You'll collaborate cross-functionally with R&D, Regulatory Affairs, Quality Assurance, and Clinical Development, while also working closely with CROs, academic partners, and global regulatory authorities.

This is a strategic, science-driven position where your deep expertise will directly influence product safety, performance, and success in global markets.



Your main responsibilities

* Define biological risks and shape preclinical strategy for injectable medical devices
* Design, coordinate and interpret preclinical safety and biocompatibility studies
* Ensure compliance with ISO 10993 series, FDA guidance, EU MDR and global regulations
* Write, review, and deliver high-quality scientific documentation: protocols, reports, and regulatory submissions (e.g., IDE, 510(k), CE marking)
* Act as preclinical lead in cross-functional projects and external collaborations
* Contribute to risk assessments per ISO 14971 and biological evaluations per ISO 10993-1
* Monitor scientific and regulatory developments in biomaterials and injectables



What we're looking for

We're seeking an experienced scientific leader who thrives at the intersection of regulatory science, toxicology, and medical device development.

Must-have qualifications:

* Ph.D. (or equivalent) in Biomedical Sciences, Toxicology, Pharmacology, Bioengineering or similar
* 6-10 years of experience in preclinical development of medical devices, preferably injectables
* Proven expertise in ISO 10993, GLP, EU MDR, and FDA regulatory requirements
* Strong background in biocompatibility testing and toxicological risk assessment
* Experience managing CROs and outsourced preclinical studies
* Excellent scientific writing and communication skills
* Fluent in English (Swedish is a plus)



Ready to make a real-world impact?

Apply now and take the lead in driving scientific excellence and patient safety in one of the world's most exciting areas of dermatology.

???? Bring your science. Shape the future. Visa mindre

Team Leader
Location: Uppsala, Sweden (on-site, skiftgång)



Jobb beskrivning

Nu söker vi en Team Leader till produktion på Lina 4 downstream. Tjänsten är riktad till den delen av linan som fokuserar på nedströmsflödet där arbetet innefattar syning, kapselresning, packning och serialisering. I ditt uppdrag inom skiftlaget har du en tydlig ledarroll där du tillsammans med övrig arbetsledning säkerställer de dagliga leveranserna inom produktionen. Du har en viktig roll mellan produktion och andra avdelningar inom verksamheten.



Ansvarsområden

Utöver det operativa arbetet i produktionen innebär teamledarens ansvar bland annat:

Leda skiftet i den dagliga produktionen mot uppsatta leverans- och arbetsmiljömål

· Leda uppstarts- och pulsmöten enligt teir-strukturen

· Aktivt delta i daglig drift och produktion

· Aktivt delta i förbättringsarbete och leda 5S aktiviteter samt förbättringsarbeten

· Eskalera driftavbrott, delta i felsökningar och arbeta proaktivt för att förhindra produktionsstopp

· Ansvara för utbuildning och att nå uppsatta certifikatsmål



Kvalifikationer

· Gymnasieutbildning

· Dokumenterad erfarenhet inom tillverkning

· Svenska och engelska i tal och skrift

Meriterande

· Ledarskapserfarenhet från formell eller informell verksamhet

· Erfarenhet från kvalitetsfrågor

· LEAN, GMP och 5S



Du förväntas arbeta för att främja laganda och engagemang hos dina medarbetare för att nå verksamhetens mål. Arbetet kräver lyhördhet, samarbetsförmåga och integritet.



Övrigt

Tjänsten innebär arbete på två-skift.



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.



Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss i moderna lokaler utmed vackra Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag, dock senast den 22 december 2025. Urval och intervjuer görs löpande under ansökningstiden, tjänsten kan komma att tillsättas innan sista ansökningsdatum.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren
* Nästa steg är en intervju med anställande chef på plats på kontoret hos Galderma
* Slutligen genomförs en referenstagning innan ett eventuellt erbjudande lämnas



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Do you have deep experience in aseptic manufacturing and visual inspection systems? Are you comfortable stepping in as a subject matter expert when complex technical challenges arise? Galderma is now hiring a Senior Process Engineer with a focus on Aseptic Filling & Visual Inspection to support our continued growth and expansion.



About the role



As Senior Process Engineer, you will work as a subject matter expert (SME) in aseptic filling and visual inspection systems for both pre-filled syringes and vials. You'll play a key role in technical projects, equipment qualification, and process development. The role requires both hands-on expertise and strong collaboration across functions such as Production Engineering, Maintenance, Automation, and Quality.

You'll contribute to the evolution of our filling and inspection capabilities by supporting investigations, leading or participating in projects, and ensuring that systems and equipment are compliant, efficient, and fit for purpose.



Key responsibilities include:

* Lead and contribute to engineering projects related to aseptic filling and visual inspection of pre-filled syringes and vials
* Act as technical owner for filling and inspection equipment and associated specifications
* Provide technical input in deviation handling and root cause investigations
* Support design, procurement, and qualification of new or modified systems
* Collaborate across departments to support manufacturing improvements and regulatory compliance



What we're looking for



You have a university degree in engineering or equivalent practical experience and bring 10+ years of experience from pharmaceutical manufacturing environments. Your expertise lies in aseptic filling and visual inspection, with a solid understanding of Grade A cleanroom standards and cGMP compliance.

You're analytical, detail-oriented, and confident in handling technical investigations and process improvements. You collaborate well across teams, communicate clearly, and take initiative when challenges arise. Fluency in English is required. Apart from this we would appreciate if you bring the following:

* Experience with CAPEX projects related to filling or inspection equipment
* Involvement in equipment commissioning and qualification
* Familiarity with Part 11 compliance and automated systems
* Experience working with external equipment suppliers
* Swedish language skills



Why Galderma?



Galderma is in a period of significant growth, investing in new manufacturing capabilities and expanding internal production. That means the work goes beyond maintaining existing systems - there's a strong focus on designing, implementing, and improving new manufacturing lines and equipment.

The engineering work is technically demanding, involving aseptic manufacturing, cleanroom environments, and compliance with pharmaceutical and medical device regulations. It requires a high level of precision and problem-solving ability.

This position offers variety: no two days look the same and the process engineer is called upon when there are complex problems to solve, new equipment to bring in, or processes to improve. Visa mindre

Job Title: Manager MSAT Device Injectables Location: Uppsala, Sweden (Hybrid)

We are looking for a passionate and strategic Manager Devices and Injectables to join our world-class MS&T organization in Uppsala. This is a unique opportunity to lead the technical strategy, process excellence, and lifecycle management for Galderma's most advanced injectable and device products - shaping global launches, driving innovation, and ensuring manufacturing performance that impacts millions of patients worldwide.

At Galderma, you won't just take on a job - you'll contribute to science-driven solutions, guide a high-performing team, and build the next generation of manufacturing capability. If you're ready to combine leadership with meaningful impact, this is the role for you.

About Galderma

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of flagship brands and services across Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology.

Since 1981, we have dedicated our focus and passion to the human body's largest organ - the skin. By understanding that the skin we are in shapes our lives, we are advancing dermatology for every skin story.

Job Description

As Manager Devices and Injectables, you will lead the technical lifecycle management of Devices and Injectables and act as a key driver for robust manufacturing processes. You will serve as a technical authority, ensure compliance with global regulatory expectations, and lead a team of MS&T specialists dedicated to injectable and device manufacturing.

Your focus will span process validation, tech transfer, CPV, troubleshooting, investigations, and continuous improvement - forming the backbone of safe, high-quality, and efficient production.

Key Responsibilities

As the Manager Devices and Injectables, you will drive technical strategy and operational excellence across manufacturing processes. Acting as a technical authority, you will ensure products are manufactured safely, efficiently, and in full compliance with global standards.

You will lead and support new product introductions, major technology transfer activities, and product remediation initiatives, while ensuring process knowledge is maintained and continuously improved. A core part of your role is to assess the impact of manufacturing changes, define and track technical CAPAs, and provide MS&T expertise during deviations, investigations, and technical complaints.

You will develop and execute process validation and revalidation strategies, author and review protocols and reports, and oversee ongoing continued process verification and annual product reviews. Your analyses will feed into recommendations for corrective actions and long-term improvements.

Collaboration is central: you will work closely with Production, Quality, Engineering, R&D, and global partners to resolve shop-floor challenges, support change controls, lead risk assessments, and provide technical insight during supplier evaluations.

As a people leader, you will mentor and develop MS&T scientists, fostering an inclusive, collaborative environment where expertise grows and accountability thrives. You ensure operational continuity by delegating effectively and building a resilient, high-performing team.

Key Requirements & Qualifications

To succeed in this role, you bring a strong mix of technical depth, leadership capability, and regulatory understanding within pharmaceutical and medical device manufacturing, particularly in Devices and Injectables. You are comfortable navigating a global environment and balancing strategic decision-making with hands-on technical support.

You likely have 10+ years of experience in pharma or medical device manufacturing, ideally with exposure to Devices and Injectables, fill-finish, or related processes, and at least 3 years of managerial experience, guiding technical experts or cross-functional teams.

Your background includes a solid foundation in manufacturing science and technology, experience in technology transfer, and a strong track record in process validation (PPQ, CPV) and lifecycle management. You are well-versed in GMP, ISO 13485, ICH, and global regulatory expectations, and have led investigations, performed root-cause analyses, implemented CAPAs, and contributed to regulatory submissions (IND, BLA, NDA, or variations).

Core competencies include:

* Leading technology transfers from development to commercial manufacturing
* Designing, executing, and reviewing process validation and revalidation protocols
* Managing deviation investigations and implementing CAPAs
* Supporting regulatory submissions and compliance inspections
* Collaborating across matrix and international teams

Strong communication skills, the ability to explain complex technical topics to diverse stakeholders, and fluency in English are essential.

Additional strengths that are highly beneficial include experience with structured problem-solving tools (FMEA, Ishikawa, 5 Whys), global or cross-border technology transfers, project management certifications (PMP, PRINCE2), and Swedish language skills.

Why Join Galderma in Uppsala?

Our Uppsala site is Galderma's Global Center of Excellence for Aesthetics - home to over 800 professionals across R&D, manufacturing, engineering, and clinical development. Here, science meets real-world application and innovation becomes product reality.

What we offer: Career development & learning opportunities, Attractive benefits and bonus programs, High-impact Devices and Injectables projects, A global & inclusive culture, Strong team spirit and engagement, Work-life balance & wellbeing initiatives

Are You the One We're Looking For?

At Galderma, we empower employees, develop strengths, and celebrate diversity. Here, you will grow your career, expand your expertise, and make a difference. Visa mindre

Job Title: Process Development Engineer, Biologics (Drug Substance or Drug Product)

Location: Uppsala, Sweden (Hybrid)



Job description :

We are looking for a new member to the Biologics team within Manufacturing Science and Technology. The Process Development Engineer is a subject matter expert (SME) responsible for new product implementation (NPI) into a manufacturing facility.



Key responsibilities:

*

Support new product implementation (NPI) strategy and all aspects of process validation, including process data reviews, investigations, risk management, and change implementation. Write validation documentation and execute process validation under guidance from senior scientists.
*

Serve as a technical SME representing MSAT in Technology Transfer projects.
*

Process owner to support day-to-day operations with a focus on continuous improvements. Identify opportunities for process enhancement, cost reduction, and efficiency gains, proactively driving necessary changes.
*

Lead and participate in investigations into deviations, incidents, and anomalies within the manufacturing process. Conduct in-depth root cause analysis to identify the underlying reasons for deviations and incidents, focusing on process improvement.
*

Collect data from various sources, including quality control reports, production logs, and other relevant documents, to support investigations and continuous process verification (CPV)
*

Write and review technical documentation ensuring compliance with regulatory and quality standards.
*

Coordinate with other experts and collaborate with cross-functional teams, including production, quality assurance, regulatory affairs, and process development, to ensure thorough investigation and timely issue resolution. Assist senior scientists in information gathering to support research studies and claims, and provide input to risk assessments/FMEAs.
*

Prepare detailed investigation reports, conveying findings and recommendations to management and relevant stakeholders



Skills & Qualifications

*

BSc or MSc in a relevant scientific or engineering field, such as Chemistry, Biochemistry, Chemical Engineering, or related discipline
*

Minimum of 2 years of experience in a biopharmaceutical environment
*

Familiarity with manufacturing processes in the biopharmaceutical industry
*

Experience in investigative methodologies and root cause analysis techniques





What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



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 600 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.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Location: Uppsala

Employment type: Full-time

Join Galderma, a leading global dermatology company with a strong international presence and a commitment to innovation, collaboration, and excellence. We offer exciting opportunities for personal and professional development in a dynamic and purpose-driven environment.



The Role

We are seeking a Quality Control Specialist - Analytical Methods, Protein to join our Quality Control (QC) organization. In this senior expert role, you will act as the technical authority in protein-based analytical methods, providing guidance, training, and scientific support to QC colleagues, cross-functional departments, and Galderma's global network. You will ensure analytical methods and laboratory practices comply with GMP and internal quality standards, lead method validations, and drive continuous improvement and optimization within your area of expertise. This position offers an exciting opportunity for an experienced professional with deep technical knowledge and a passion for analytical excellence and quality.



Key Responsibilities

* Serve as Subject Matter Expert (SME) in analytical methods for proteins, including chromatographic, electrophoretic, and spectroscopic techniques.
* Provide technical leadership, training, and mentorship to QC analysts and cross-functional partners.
* Lead and coordinate method validations, including design, execution, evaluation, and reporting.
* Ensure analytical methods and QC operations comply with GMP, GxP, and Galderma quality standards.
* Identify, assess, and mitigate quality and compliance risks; support investigations with technical expertise.
* Represent QC in cross-functional and global projects, providing analytical insights and recommendations.
* Drive continuous improvement and simplification of analytical methods, work instructions, and quality systems.
* Prepare and present technical documentation and reports for audits, inspections, and internal/external stakeholders.
* Contribute to a positive, compliant, and collaborative laboratory culture.



Your Profile

Education:

* PhD or Master's degree (or equivalent) in Biochemistry, Biotechnology, or a related field.

Experience:

* Minimum 10 years of experience in Quality Control or R&D with a focus on protein analytical methods.
* Extensive laboratory experience in chromatographic, electrophoretic, or spectroscopic analysis of proteins (e.g., SE, SEC-HPLC, SDS-PAGE, Western Blot).
* Strong knowledge of method development, optimization, and validation.
* Documented experience with GxP, GMP, and regulatory requirements for pharmaceuticals and/or medical devices.
* Proven ability to train, coach, and explain complex analytical concepts to internal and external audiences.

Skills:

* Advanced problem-solving and project management abilities.
* Strong communication and presentation skills in English and Swedish (both written and spoken).
* Ability to work independently and collaboratively in a global, cross-functional environment. Visa mindre

Location: Uppsala

Employment type: Full-time



The Role

We are seeking a Quality Control Specialist - Molecular Biological Methods to join our Quality Control (QC) organization. In this senior expert role, you will act as the technical authority for molecular biological analytical methods, providing scientific guidance, training, and support to QC colleagues, cross-functional departments, and Galderma's global network. You will ensure analytical methods and laboratory routines comply with GMP and internal quality standards, lead method validations, and drive continuous improvement and optimization initiatives. This position is ideal for an experienced professional with a deep understanding of molecular biological methods and a passion for quality, compliance, and innovation.



Key Responsibilities

* Serve as Subject Matter Expert (SME) in molecular biological methods such as Western Blot and cell-based assays, including troubleshooting, optimization, and method development.
* Provide technical leadership, training, and mentorship to QC team members and other internal stakeholders.
* Lead and coordinate method validations, including set-up, performance, data analysis, and reporting.
* Ensure analytical methods and QC operations comply with GMP, GxP, and Galderma quality standards.
* Identify and mitigate quality and compliance risks; contribute to investigations and root cause analyses with advanced technical insight.
* Represent QC in cross-functional and global projects, providing scientific expertise and recommendations.
* Drive continuous improvement and simplification of analytical methods, work instructions, and quality systems.
* Prepare and deliver technical presentations, reports, and documentation for internal and external stakeholders, including regulatory inspections.
* Promote a collaborative, compliant, and quality-focused laboratory culture.



Your Profile

Education:

* PhD or Master's degree (or equivalent) in Molecular Biology, Biochemistry, Biotechnology, or a related field.

Experience:

* Minimum 10 years of experience in Quality Control or R&D, with a focus on molecular biological methods and analytical development.
* Extensive experience in techniques such as Western Blot, ELISA, and cell-based assays, including troubleshooting and optimization.
* Proven experience with GxP, GMP, and pharmaceutical and/or medical device regulations.
* Demonstrated ability to train, mentor, and clearly communicate technical concepts to diverse audiences.

Skills:

* Advanced problem-solving and analytical thinking skills.
* Strong project management and cross-functional collaboration abilities.
* Excellent communication and presentation skills in Swedish and English (written and spoken).
* Ability to work independently and proactively in a complex, global environment. Visa mindre

Job Title: Senior Sterilization Process Development Scientist/Engineer

Location: Uppsala, Sweden, On-site



Job Description

Are you an experienced aseptic processing professional with experience in the sterilization of pharmaceuticals or medical devices? If so, this could be the role for you as we are now hiring a Senior Scientist/Engineer in our Injectable Development team.

Elevate your career by joining Galderma for a role that involves subject-matter expertise in the field of sterilization process development and process transfer to manufacturing facilities for both injectable medical devices and pharmaceuticals. As an integral part of the Product Science department, you will be highly involved in developing new products to further expand Galderma's portfolio and building our parenteral technology capabilities.



Key responsibilities

* Act as a steam sterilization Subject Matter Expert (SME) for projects and provide required experimental designs, data and author technical reports compliant with regulatory guidelines and industrial standards.
* Lead activities related to sterilization process development of injectable products under development, including work with regulatory submissions, design control, specifications, and risk assessments.
* Represent the Process Science team in cross functional product development teams with other internal departments and external manufacturing partners.
* Participate in key Product Science activities to assess impact of new regulations and implement appropriate changes
* Keep up to date with innovations in aseptic and low bioburden processing, share and implement new technology in the organization.



Skills & Qualifications

* Expertise in development and validation of Steam-In-Place and terminal sterilization for parenteral products using steam/moist heat
* Experience with sterilization using irradiation methods is also desirable
* Strong knowledge in microbiological controls and the use of biological indicators including risk assessment, validation and environmental monitoring techniques
* Knowledge of cGMP and Design Control in regulatory controlled work environments (e.g. ISO 13485, 21 CFR820, ICHQ8, 21CFR210/211, etc.) and experience preparing regulatory filings and supporting documentation
* Fluent in English, ability to work in Swedish is also desirable.
* Strong communication skills, providing guidance and information to internal and external stakeholders and talking with regulatory bodies during inspections
* University degree in Chemical or Mechanical Engineering, Chemistry, Biochemistry, Biotechnology or similar technical field and 8 years experience in the pharmaceutical or medical device field.



What We Offer

At Galderma, we believe that our people are our most valuable asset and we are committed to creating an environment where you can thrive both professionally and personally.

When you join us, you can expect:

Competitive Compensation & Career Growth: Attractive salary and benefits, continuous learning and clear opportunities for advancement. Work on innovative projects that make a real difference in people's lives.

Global & Inclusive Culture: Collaborate across sites in North America, South America, and Europe in a diverse and inclusive environment that values teamwork and different perspectives.

Work-Life Balance & Wellbeing: Flexible working hours, wellness initiatives and on-site amenities including a fully equipped gym in a beautiful location by the river Fyris, just 10 minutes by bike from Uppsala city center.

Social Engagement & Team Spirit: Participate in an active leisure and sports club, enjoy quarterly town halls with fika, employee-led summer parties and celebrate key milestones such as Yellow Belt certifications together.



Next Steps

We welcome your application via our company website CAREERS | Galderma. Please apply as soon as possible as the selection process is ongoing and applications will be reviewed continuously.

If your profile matches our requirements, you will be invited to an initial virtual call with the recruiter.

The next step will be an interview with the hiring manager.

Then follows a panel discussion with the extended team.

Finally, a reference check is carried out before a possible offer is made.



We wish to inform applicants 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. Visa mindre

Job Title: Manager MSAT Device Injectables

Location: Uppsala, Sweden (Hybrid)



Job description:

In this exciting leadership role, you'll manage a skilled team of scientists working with Device Injectables - focused on both new product implementation (NPI) and commercial production support.

Together, you'll turn cutting-edge technologies into real-world manufacturing capabilities by applying science, solving problems, and driving continuous improvement.

You'll play a key part in bridging innovation and production - ensuring that what's developed in R&D can be scaled, validated, and successfully transferred to manufacturing.



Key responsibilities:

As Manager MSAT Device Injectables, you and your team will:

*

Lead NPI activities - from early prototyping to full-scale manufacturing
*

Ensure smooth tech transfer from R&D into commercial production
*

Own and optimize end-to-end assembly and packaging processes
*

Ensure design solutions from engineering teams support manufacturing efficiency, reliability, and quality
*

Develop and validate processes for bulk and fill-finish manufacturing of injectable device products
*

Drive process validation (PV), trending, and continuous process verification (CPV)
*

Provide expert technical support for daily operations, audits, and regulatory submissions
*

Own change controls and ensure compliance with all relevant regulatory frameworks (LoRR, MDR, etc.)
*

Be responsible for process material specifications and post-validation documentation
*

Own design control documentation after product transfer to production



In this role, you'll collaborate closely with QA, Engineering, R&D, Regulatory Affairs, and external partners - helping to solve complex challenges and enable seamless production.

You'll also serve as a trusted advisor to senior leaders, guiding them on best practices, systems, and process strategies to ensure high performance across functions.

Skills & Qualifications

We're looking for a pragmatic, hands-on leader with a deep understanding of injectable manufacturing - someone who thrives where science meets execution and isn't afraid to take technical ownership.

You bring experience from the shop floor to senior decision-making, and you know how to drive products from R&D into full-scale production - efficiently, compliantly, and collaboratively.



You're likely a great match if you have:

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8+ years in biopharma or medical device manufacturing, especially with injectables
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Solid knowledge of bulk formulation, sterile filtration, fill-finish (syringes, vials), visual inspection, and sterilization
*

Strong background in tech transfer, process validation (IQ, OQ, PQ, PPQ, FAT, SAT), and commercial manufacturing
*

Hands-on experience managing CAPA, deviations, audits, and documentation ownership
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Proven ability to lead process implementation, equipment qualification (including URS), and supplier collaboration - ideally with CAPEX exposure
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Familiarity with GMP, ISO 13485, 21 CFR Part 11, and MDR
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End-to-end process responsibility: from design input to commercial readiness
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Leadership experience with at least 2 direct reports
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Excellent communicator, confident across functions like QA, R&D, Production, and Engineering
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Fluent in English (Swedish is a plus)



Bonus points if you bring:

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Skills in problem-solving frameworks (e.g. 5 Whys, FMEA, Ishikawa)
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Experience in global or matrix-driven organizations
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A project management certification (PMP, PRINCE2, or equivalent)

Why Join Galderma in Uppsala?

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics - home to over 800 professionals working across R&D, manufacturing, clinical development, and marketing, all under one roof.

You'll be part of a multidisciplinary team where science meets application.



What we offer:

· Career development & learning opportunities

· Attractive benefits and bonus models

· Innovative projects

· Global & inclusive culture

· Strong team spirit & engagement

· Work-life balance & wellbeing



Are You the One We're Looking For?

We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact. Visa mindre

Do you have deep experience in aseptic manufacturing and visual inspection systems? Are you comfortable stepping in as a subject matter expert when complex technical challenges arise? Galderma is now hiring a Senior Process Engineer with a focus on Aseptic Filling & Visual Inspection to support our continued growth and expansion.



About the role



As Senior Process Engineer, you will work as a subject matter expert (SME) in aseptic filling and visual inspection systems for both pre-filled syringes and vials. You'll play a key role in technical projects, equipment qualification, and process development. The role requires both hands-on expertise and strong collaboration across functions such as Production Engineering, Maintenance, Automation, and Quality.

You'll contribute to the evolution of our filling and inspection capabilities by supporting investigations, leading or participating in projects, and ensuring that systems and equipment are compliant, efficient, and fit for purpose.



Key responsibilities include:

* Lead and contribute to engineering projects related to aseptic filling and visual inspection of pre-filled syringes and vials
* Act as technical owner for filling and inspection equipment and associated specifications
* Provide technical input in deviation handling and root cause investigations
* Support design, procurement, and qualification of new or modified systems
* Collaborate across departments to support manufacturing improvements and regulatory compliance



What we're looking for



You have a university degree in engineering or equivalent practical experience and bring 10+ years of experience from pharmaceutical manufacturing environments. Your expertise lies in aseptic filling and visual inspection, with a solid understanding of Grade A cleanroom standards and cGMP compliance.

You're analytical, detail-oriented, and confident in handling technical investigations and process improvements. You collaborate well across teams, communicate clearly, and take initiative when challenges arise. Fluency in English is required. Apart from this we would appreciate if you bring the following:

* Experience with CAPEX projects related to filling or inspection equipment
* Involvement in equipment commissioning and qualification
* Familiarity with Part 11 compliance and automated systems
* Experience working with external equipment suppliers
* Swedish language skills



Why Galderma?



Galderma is in a period of significant growth, investing in new manufacturing capabilities and expanding internal production. That means the work goes beyond maintaining existing systems - there's a strong focus on designing, implementing, and improving new manufacturing lines and equipment.

The engineering work is technically demanding, involving aseptic manufacturing, cleanroom environments, and compliance with pharmaceutical and medical device regulations. It requires a high level of precision and problem-solving ability.

This position offers variety: no two days look the same and the process engineer is called upon when there are complex problems to solve, new equipment to bring in, or processes to improve. Visa mindre

Maintenance Technician
Location: Uppsala, Sweden (on-site)



Arbetsbeskrivning
Vi söker en underhållstekniker för att stödja och förbättra vår verksamhet inom Engineering. Du kommer att vara involverad i att implementera planer, förbättra processer och samarbeta i innovativa projekt som driver vår verksamhet framåt.



Ansvarsområden

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Implementera tekniska planer och program för att stödja operativa aktiviteter inom olika tekniska funktioner.
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Spåra och anpassa aktiviteter för att förbättra processer, modifiera befintliga system och utveckla effektiva testprocedurer.
*

Utföra tekniska processer och policyer, med fokus på utveckling av nya produkter och förbättring av befintliga.
*

Analysera tekniktrender och säkerställ framgångsrik implementering av tekniska planer samtidigt som du följer kvalitets-, kostnads- och säkerhetsstandarder.
*

Samarbeta för att bedöma teknisk genomförbarhet, kostnadseffektivitet och kundernas efterfrågan på produkter och processer.
*

Delta i fälttester av produkter, processer och system för att säkerställa tillförlitlighet och prestanda.
*

Underhåll och förbättra utrustning genom att felsöka problem, utföra förebyggande underhåll och säkerställa drifteffektivitet.



Kvalifikationer

*

Högskoleutbildning inom relevant område eller motsvarande erfarenhet/behörighet.
*

Viss erfarenhet inom praktiska ingenjörsuppgifter. Det är en fördel om du har erfarenhet inom styr- och regler, och/eller el.
*

Flytande svenska och engelska.
*

B-körkort.
*

Stark analytisk och problemlösningsförmåga med känsla för detaljer.
*

Förmåga att samarbeta effektivt med kollegor och bidra till tvärfunktionella team.
*

Kännedom om tekniska standarder, säkerhetsprotokoll och kvalitetssäkring.
*

Nyfiken på att lära sig och anpassa sig till ny teknik och tekniska trender.



Övrig information

Skiftgång och/eller beredskap kan förekomma.



Vi erbjuder
Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.



I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.



På Galderma i Uppsala har vi verksamhet inom produktutveckling och tillverkning inom dermatologi och vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Vi är belägna längs med Fyrisån i Uppsala, 10 minuters cykelfärd från Uppsala Resecentrum.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag. Urval och intervjuer görs löpande under ansökningstiden, och tjänsten kan komma att tillsättas innan sista ansökningsdatum.

*

Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren.
*

Nästa steg är en intervju med anställande chef
*

Sista steget är en panelintervju med teamet



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Job title: Aseptic Filling Operator

Location: Uppsala, Sweden



About the Role

We are looking for a dedicated and detail-oriented Aseptic Filling Operator to join our production team in Uppsala.

In this role, you will work in a cleanroom environment with aseptic manufacturing and filling processes, following established method journals, work instructions, and quality standards. You will contribute to ensuring that all products meet Galderma's high requirements for quality, safety, and traceability in accordance with GMP regulations.



This is an exciting opportunity for someone who enjoys hands-on work in a structured and collaborative setting, and who wants to be part of a company making a real impact in dermatology.



Key Responsibilities

* Perform production activities according to current method journals and handling instructions.
* Ensure that all work is performed aseptically and safely, using appropriate protective equipment.
* Accurately complete process documentation and batch records.
* Report any quality deviations or irregularities to the production supervisor.
* Conduct preventive maintenance on equipment and assist with troubleshooting during downtime.
* Maintain a high standard of order and cleanliness in the production area.
* Contribute to continuous improvement of processes and routines.
* Support competence development for yourself and your colleagues.
* Contribute to cost-efficient and quality-driven production.



Your Profile

* Completed upper secondary education (3-year program), preferably with a technical, industrial, or science focus.
* Good knowledge of Swedish and English, both spoken and written.
* Good computer skills (Word and Excel).
* Experience working in a cleanroom environment and with GMP manufacturing is an advantage.



Who You Are

* Careful, structured, and quality focused.
* Responsible and proactive, with a strong sense of teamwork.
* Curious about technology, manufacturing, and continuous improvement.
* Comfortable working in a highly regulated environment with strict hygiene and safety standards. Visa mindre

Do you have deep experience in aseptic manufacturing and visual inspection systems? Are you comfortable stepping in as a subject matter expert when complex technical challenges arise? Galderma is now hiring a Senior Process Engineer with a focus on Aseptic Filling & Visual Inspection to support our continued growth and expansion.



About the role



As Senior Process Engineer, you will work as a subject matter expert (SME) in aseptic filling and visual inspection systems for both pre-filled syringes and vials. You'll play a key role in technical projects, equipment qualification, and process development. The role requires both hands-on expertise and strong collaboration across functions such as Production Engineering, Maintenance, Automation, and Quality.

You'll contribute to the evolution of our filling and inspection capabilities by supporting investigations, leading or participating in projects, and ensuring that systems and equipment are compliant, efficient, and fit for purpose.



Key responsibilities include:

* Lead and contribute to engineering projects related to aseptic filling and visual inspection of pre-filled syringes and vials
* Act as technical owner for filling and inspection equipment and associated specifications
* Provide technical input in deviation handling and root cause investigations
* Support design, procurement, and qualification of new or modified systems
* Collaborate across departments to support manufacturing improvements and regulatory compliance



What we're looking for



You have a university degree in engineering or equivalent practical experience and bring 10+ years of experience from pharmaceutical manufacturing environments. Your expertise lies in aseptic filling and visual inspection, with a solid understanding of Grade A cleanroom standards and cGMP compliance.

You're analytical, detail-oriented, and confident in handling technical investigations and process improvements. You collaborate well across teams, communicate clearly, and take initiative when challenges arise. Fluency in English is required. Apart from this we would appreciate if you bring the following:

* Experience with CAPEX projects related to filling or inspection equipment
* Involvement in equipment commissioning and qualification
* Familiarity with Part 11 compliance and automated systems
* Experience working with external equipment suppliers
* Swedish language skills



Why Galderma?



Galderma is in a period of significant growth, investing in new manufacturing capabilities and expanding internal production. That means the work goes beyond maintaining existing systems - there's a strong focus on designing, implementing, and improving new manufacturing lines and equipment.

The engineering work is technically demanding, involving aseptic manufacturing, cleanroom environments, and compliance with pharmaceutical and medical device regulations. It requires a high level of precision and problem-solving ability.

This position offers variety: no two days look the same and the process engineer is called upon when there are complex problems to solve, new equipment to bring in, or processes to improve. Visa mindre

Preclinical Principal Scientist - Injectable Medical Devices

???? Uppsala, Sweden | Hybrid | Full-time | Permanent

Shape the future of aesthetic innovation at Galderma

At Galderma, we're not just offering a job - we're inviting you to shape the future of dermatology. As a global leader in the science of skin, we combine purpose with innovation to improve the lives of millions.

Now, we're looking for a passionate and driven Preclinical Principal Scientist to join our team in Uppsala and lead the preclinical safety strategy for our next-generation injectable medical devices. If you're ready to bring science to life and make an impact beyond the lab, this is your chance.



Why join Galderma in Uppsala?

Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 600 professionals working across R&D, manufacturing, clinical development, and marketing - all under one roof.

You'll be part of a multidisciplinary team where science meets application, with world-leading brands such as Restylane®, Azzalure®, and Sculptra®. We offer:

* A hybrid work model with flexible hours
* Continuous learning & career development opportunities
* A diverse, inclusive, and collaborative culture
* A modern workplace just 10 minutes from Uppsala Central Station



About the role

As Preclinical Principal Scientist, you'll be a key scientific leader responsible for defining and driving preclinical strategies for our injectable devices - from biocompatibility and toxicological risk assessments to supporting regulatory submissions and clinical trials.

You'll collaborate cross-functionally with R&D, Regulatory Affairs, Quality Assurance, and Clinical Development, while also working closely with CROs, academic partners, and global regulatory authorities.

This is a strategic, science-driven position where your deep expertise will directly influence product safety, performance, and success in global markets.



Your main responsibilities

* Define biological risks and shape preclinical strategy for injectable medical devices
* Design, coordinate and interpret preclinical safety and biocompatibility studies
* Ensure compliance with ISO 10993 series, FDA guidance, EU MDR and global regulations
* Write, review, and deliver high-quality scientific documentation: protocols, reports, and regulatory submissions (e.g., IDE, 510(k), CE marking)
* Act as preclinical lead in cross-functional projects and external collaborations
* Contribute to risk assessments per ISO 14971 and biological evaluations per ISO 10993-1
* Monitor scientific and regulatory developments in biomaterials and injectables



What we're looking for

We're seeking an experienced scientific leader who thrives at the intersection of regulatory science, toxicology, and medical device development.

Must-have qualifications:

* Ph.D. (or equivalent) in Biomedical Sciences, Toxicology, Pharmacology, Bioengineering or similar
* 6-10 years of experience in preclinical development of medical devices, preferably injectables
* Proven expertise in ISO 10993, GLP, EU MDR, and FDA regulatory requirements
* Strong background in biocompatibility testing and toxicological risk assessment
* Experience managing CROs and outsourced preclinical studies
* Excellent scientific writing and communication skills
* Fluent in English (Swedish is a plus)



Ready to make a real-world impact?

Apply now and take the lead in driving scientific excellence and patient safety in one of the world's most exciting areas of dermatology.

???? Bring your science. Shape the future. Visa mindre

Job Title: Senior Formulation and Filling Process Development Scientist/Engineer

Location: Uppsala, Sweden



Job Description

Are you an experienced formulation scientist or fill/finish process development professional with experience in aseptic pharmaceuticals or medical devices? If so, this could be the role for you as we are now hiring a Senior Scientist/Engineer in our Injectable Development team.

Elevate your career by joining Galderma for a role that involves subject-matter expertise in the field of protein and polymer product formulation, process development, scale up and process transfer to manufacturing facilities for both injectable medical devices and pharmaceuticals. As an integral part of the Product Science department, you will be highly involved in developing new products to further expand Galderma's portfolio and building our parenteral technology capabilities.

Key responsibilities

* Act as a Subject Matter Expert (SME) for projects and provide required experimental designs, data and author technical reports compliant with regulatory guidelines and industrial standards.
* Lead activities related to filling and sterilization processes of injectable products under development, including work with regulatory submissions, design control, specifications, and risk assessments.
* Represent the Process Science team in cross functional product development teams with other internal departments and external partners.
* Participate in key Product Science activities to assess impact of new regulations and implement appropriate changes
* Keep up to date with innovations in parenteral formulations and filling, share and implement new technology in the organization.



Skills & Qualifications

* Expertise in the formulation and process development of prefilled syringes and/or vials. Experience transferring and validating processes to internal manufacturing facilities and Contract Manufacturing Organizations (CMOs)
* Experience with biopolymers or protein characterization for injectable medical devices and/or pharmaceutical products and the development of terminal sterilization processes is desirable.
* Familiarity with filling machines and clean room environments as well as aseptic techniques and microbiological controls
* Knowledge of cGMP and Design Control in regulatory controlled work environments (e.g. ISO 13485, 21 CFR820, ICHQ8, 21CFR210/211, etc.) and experience preparing regulatory filings and supporting documentation
* Fluent in English, ability to work in Swedish is also desirable.
* Strong communication skills, providing guidance and information to internal and external stakeholders
* University degree in Chemical or Mechanical Engineering, Chemistry, Biochemistry, Biotechnology or similar technical field and 8 years experience in the pharmaceutical or medical device field.



What We Offer

At Galderma, we believe that our people are our most valuable asset and we are committed to creating an environment where you can thrive both professionally and personally.

When you join us, you can expect:

Competitive Compensation & Career Growth: Attractive salary and benefits, continuous learning and clear opportunities for advancement. Work on innovative projects that make a real difference in people's lives.

Global & Inclusive Culture: Collaborate across sites in North America, South America, and Europe in a diverse and inclusive environment that values teamwork and different perspectives.

Work-Life Balance & Wellbeing: Flexible working hours, wellness initiatives and on-site amenities including a fully equipped gym in a beautiful location by the river Fyris, just 10 minutes by bike from Uppsala city center.

Social Engagement & Team Spirit: Participate in an active leisure and sports club, enjoy quarterly town halls with fika, employee-led summer parties and celebrate key milestones such as Yellow Belt certifications together.



Next Steps

We welcome your application via our company website CAREERS | Galderma. Please apply as soon as possible as the selection process is ongoing and applications will be reviewed continuously.



If your profile matches our requirements, you will be invited to an initial virtual call with the recruiter.

The next step will be an interview with the hiring manager.

Then follows a panel discussion with the extended team.

Finally, a reference check is carried out before a possible offer is made.



We wish to inform applicants 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. Visa mindre

Job Title: Senior DP-filling Scientist
Location: Uppsala, Sweden (onsite)



Join Our Mission to Advance Biologic Drug Development - We're Hiring a Senior DP-filling Scientist



Do you want to work hands-on with the development of high-quality biological Drug Products in an innovative and science-driven environment? Are you experienced in pharmaceutical manufacturing with specific skills and knowledge in DP-filling science such as formulation, sterile filtration and filling technology for biological products with a deep understanding of all requirements around aseptic filling and ready to shape future processes that bring biologic therapies to patients?



We are currently seeking a skilled and motivated Senior DP-filling Scientist to join our expanding team. In this role, you will contribute to the development and optimization of injectable drug product processes, with a clear focus on quality, scalability, and compliance.



What You Will Do



You will be part of the Product Science & MS&T function, supporting both early and late-stage development. Your key responsibilities will include:

· Designing and optimizing processes for formulation, filtration, and filling of drug products

· Translating development work into scalable, robust manufacturing processes

· Contributing to technology transfer, troubleshooting, and process improvements

· Supporting documentation for regulatory submissions and internal quality systems

· Collaborating closely with R&D, Operations, QA, and Regulatory Affairs



What You Bring



· A Master's or Bachelor's degree in Bioprocess Engineering, Chemical Engineering, Mechanical Engineering, or a related life science field

· At least 5 years of experience, 10-15 years is meriting, in drug product development, pharmaceutical process development, or related manufacturing roles

· Strong knowledge of formulation, mixing, and drug product handling

· Experience with aseptic processing, injectable products, or biologics is highly valued but not required



Soft Skills That Matter



· You are a strong communicator with the ability to work cross-functionally and build effective relationships

· You work in a structured, analytical way and take initiative to solve problems

· You are adaptable, collaborative, and motivated by quality and continuous improvement



Why Join Us?



· Be part of a growing organization focused on innovation in biologics and injectable drug products

· Join a passionate, skilled team with strong scientific expertise and collaborative culture

· Work from our expanding site in Uppsala, with career development opportunities and modern technology platforms

Ready to take the next step in your pharmaceutical career? Apply now and help us shape the future of injectable biologics. Visa mindre

Job Title: Security Team Lead

Location: Uppsala

Number of opening: 1

About the Role

We are looking for an experienced Security Team Leader to join our team. In this role, you will be responsible for the operation, monitoring, and development of our technical security systems including CCTV, intruder alarms, and access control systems. You will also manage security-related projects, oversee budgets, and support the Head of EHS & Security in ensuring a safe and compliant workplace.

This is a hands on role where you'll work independently, coordinate with internal and external stakeholders, and provide expert security guidance across the organization.

Key Responsibilities

* Monitor and manage technical security systems (CCTV, alarms, access systems).
* Ensure compliance with Swedish legislation and company security policies.
* Lead projects for the expansion and replacement of security systems.
* Manage and supervise the security department budget in collaboration with the Head of EHS & Security.
* Oversee contracts and orders for technical systems, security guards, and patrol services.
* Develop and update security routines, instructions, and internal controls.
* Deliver security training for employees, consultants, and contractors.
* Support and participate in threat and security investigations.
* Provide personal risk and security advice to managers and staff.
* Collaborate with IT, other departments, contractors, and external suppliers to ensure effective security operations.
* Take part in scheduled on-call duty.


What We're Looking For

* Bachelor's degree or equivalent qualification in a relevant field.
* 3-5+ years of experience in security operations, technical systems, or a related area.
* Strong knowledge of CCTV, alarms, and access control systems.
* Knowledge of the Protective Security Act and its practical application in a corporate environment.
* Proven experience in project management and budget handling.
* Excellent communication and stakeholder management skills.
* Fluent in Swedish and English (spoken and written).
* Ability to work independently, with a structured and proactive approach.



What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.

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 600 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. Visa mindre

Job Title: Senior Formulation and Filling Process Development Scientist/Engineer

Location: Uppsala, Sweden



Job Description

Are you an experienced formulation scientist or fill/finish process development professional with experience in aseptic pharmaceuticals or medical devices? If so, this could be the role for you as we are now hiring a Senior Scientist/Engineer in our Injectable Development team.

Elevate your career by joining Galderma for a role that involves subject-matter expertise in the field of protein and polymer product formulation, process development, scale up and process transfer to manufacturing facilities for both injectable medical devices and pharmaceuticals. As an integral part of the Product Science department, you will be highly involved in developing new products to further expand Galderma's portfolio and building our parenteral technology capabilities.

Key responsibilities

* Act as a Subject Matter Expert (SME) for projects and provide required experimental designs, data and author technical reports compliant with regulatory guidelines and industrial standards.
* Lead activities related to filling and sterilization processes of injectable products under development, including work with regulatory submissions, design control, specifications, and risk assessments.
* Represent the Process Science team in cross functional product development teams with other internal departments and external partners.
* Participate in key Product Science activities to assess impact of new regulations and implement appropriate changes
* Keep up to date with innovations in parenteral formulations and filling, share and implement new technology in the organization.



Skills & Qualifications

* Expertise in the formulation and process development of prefilled syringes and/or vials. Experience transferring and validating processes to internal manufacturing facilities and Contract Manufacturing Organizations (CMOs)
* Experience with biopolymers or protein characterization for injectable medical devices and/or pharmaceutical products and the development of terminal sterilization processes is desirable.
* Familiarity with filling machines and clean room environments as well as aseptic techniques and microbiological controls
* Knowledge of cGMP and Design Control in regulatory controlled work environments (e.g. ISO 13485, 21 CFR820, ICHQ8, 21CFR210/211, etc.) and experience preparing regulatory filings and supporting documentation
* Fluent in English, ability to work in Swedish is also desirable.
* Strong communication skills, providing guidance and information to internal and external stakeholders
* University degree in Chemical or Mechanical Engineering, Chemistry, Biochemistry, Biotechnology or similar technical field and 8 years experience in the pharmaceutical or medical device field.



What We Offer

At Galderma, we believe that our people are our most valuable asset and we are committed to creating an environment where you can thrive both professionally and personally.

When you join us, you can expect:

Competitive Compensation & Career Growth: Attractive salary and benefits combined with leadership programs, continuous learning and clear opportunities for advancement. Work on innovative projects that make a real difference in people's lives.

Global & Inclusive Culture: Collaborate across sites in North America, South America, and Europe in a diverse and inclusive environment that values teamwork and different perspectives.

Work-Life Balance & Wellbeing: Flexible working hours, wellness initiatives and on-site amenities including a fully equipped gym in a beautiful location by the river Fyris, just 10 minutes by bike from Uppsala city center.

Social Engagement & Team Spirit: Participate in an active leisure and sports club, enjoy quarterly town halls with fika, employee-led summer parties and celebrate key milestones such as Yellow Belt certifications together.



Next Steps

We welcome your application via our company website CAREERS | Galderma. Please apply as soon as possible as the selection process is ongoing and applications will be reviewed continuously.



If your profile matches our requirements, you will be invited to an initial virtual call with the recruiter.

The next step will be an interview with the hiring manager.

Then follows a panel discussion with the extended team.

Finally, a reference check is carried out before a possible offer is made.



We wish to inform applicants 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. Visa mindre

Om rollen:

Som Launch-projektledare driver, planerar och följer du upp lanseringsprojekt och ändringsärenden för projekt i enlighet med våra interna processer. Arbetet utförs enligt gällande myndighetskrav (ISO 13485 och cGMP) och du är ansvarig för leverabler och tidslinjer för dina projekt. Övriga arbetsuppgifter är bland annat att:

* Kommunicera status för projekten
* Se till att Project Management, Supply chain, Regulatory och övriga funktioner informeras om effekterna av relevanta förändringar som kan påverka deras verksamhet
* Delta i projekt med nya produkter/produktförändring och fungera som gränssnitt för supply chain-funktionerna
* Administrera och samordna ändringsärenden enligt instruktioner
* Utvecklar strategier relaterade till de change control-ärenden som hanteras, för att säkerställa och driva en effektiv implementering



Är du den vi söker?

Lämplig bakgrund för den här rollen är ingenjörsexamen i kemiteknik, apotekarexamen eller annan högre naturvetenskaplig utbildning. Du har också minst två års erfarenhet från Medical Device/läkemedel eller liknande bransch samt minst två års erfarenhet av koordinering av större aktiviteter eller projektledning inom Life Science. Du har en dokumenterad erfarenhet av att driva ändringsärenden samt arbete enligt GMP. Då arbetet innebär mycket kontakter krävs god kommunikativ förmåga såväl på svenska som på engelska.



Det är meriterande om du har erfarenhet av försörjningsprojekt och försörjningsprocesser, Trackwise. processutveckling i en tillverkande industri, inköp av utrustningar till en tillverkande industri samt en förståelse för regulatoriska processer.



Då rollen innebär att du har flera projekt som du driver samtidigt bör du tycka att det är kul med utmaningar och du behöver vara bra på att planera din egen tid. Du har förmåga att arbeta flexibelt och göra problem till lösningar på ett strukturerat sätt samt driva aktiviteter i mål. Samarbete och effektiv kommunikation är också viktiga attribut i den här rollen.



Vad vi erbjuder:

I Uppsala ligger Galdermas globala center för affärsområdet Aesthetics (estetik) med verksamhet inom produktutveckling och tillverkning. Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss utmed Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg?

* Om din profil stämmer överens med kravprofilen, kommer du att bli inbjuden till ett inledande virtuellt samtal med rekryteraren.

* Nästa steg är ett virtuellt samtal med den rekryterande chefen.

* Det avslutande steget är ett möte med teamet där även uppdraget presenteras.

Urval sker löpande, så vänta inte med din ansökan! Visa mindre

At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.



Job Title: Sr Microbiological Scientist

Location: Uppsala, Sweden, On-site



Job Description

Are you a Microbiologist with experience from working with medical device or pharmaceuticals? Do you want to work as a Senior Microbiologist in a global organization that is currently in an exciting and expansive phase? Then this can be the role for you!

The newly implanted Microbiology Development team, a part of the Injectable Aesthetics Development department in Uppsala, and is responsible for the microbiological expertise in the development of new products to further expand Galderma´s portfolio. To this positive and engaged group we are now looking for a Senior Microbiologist.



About the role

As Senior Microbiologist, you will plan and perform analytical tasks and you will evaluate and discuss the results. Work is performed according to regulatory requirements (ISO 13485 and GMP) and is often conducted in project form. Together with the experienced team you will work to solve advanced analytical tasks, develop and validate analytical methods. You ensure all work is performed in accordance with industry standards and regulatory requirements. You will develop and validate new microbiological methods. You will perform analysis of products, API's, intermediates and raw materials using different analytical techniques.

We offer an evolving and diverse job with opportunities in many different projects and interactions with several parts of our organization. For the right person there are great opportunities to evolve both personally and technically within the role.



Key responsibilities as Sr Analytical Scientist

* Development and validation of analytical methods
* Write protocols, reports, SOPs and technical documentation
* Provide expert microbiological support in cross-functional projects and work streams
* Ensure all work is performed in accordance with industry standards, guidelines and regulatory requirements.
* Ensure appropriate reporting and documentation of activities and project progression. Provide technical and science-based solutions to projects.



Skills & Qualifications

We believe that you have an education within Microbiology or Molecular biology and additional experience from working in the medical device or pharmaceutical industry.



We think that you have the following skills and competences:

* Proficiency within microbiology (either a broad general knowledge of several techniques or specific expert knowledge)
* Experience from method development and validation.
* Experience from regulatory controlled work/processes (e.g. ISO 13485, 21 CFR820 or similar for drug development) and interpretation of pharmacopeia's and international standards and guidelines.
* Fluent in English and Swedish, oral and written.
* Experience with cell banking is a merit.
* Experience with sequencing/bioinformatics is a merit.
* Experience with microbiology regarding sterilization of medical device/pharma products is a merit.



As a person you are ambitious and goal oriented. You are organized and work independently.



What We Offer

* Work in an exciting international environment
* Competitive salary and benefits.
* A collaborative and inclusive work culture.
* A chance to contribute to the global success of Galderma.



Don't miss this opportunity to elevate your career with Galderma! Apply now to be part of our dynamic team shaping the future of injectable aesthetics.



Your application

You are welcome to send your application (CV and letter) in English or Swedish as soon as possible though no later than 2025-09-15 to Elisabeth Thulin. Interviews with candidates can start before that date. Should you have questions about this opportunity you are welcome to contact recruiting manager Elisabeth Thulin (Manager Microbiology Development) on phone number 076-898 12 82.



We wish to inform applicants 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. Visa mindre

Automationsingenjör till Galderma Uppsala



Vill du arbeta som Automationsingenjör i en global organisation som just nu är inne i en spännande och kraftigt expansiv fas? Vill du vara en del utav en verksamhet som bidrar till människors välmående? Då är antagligen den här rollen något för dig - vi på Galderma i Uppsala behöver en till automationsingenjör!



Om rollen

Som automationsingenjör ingår du i gruppen Production Engineering, vars ansvar är att förvalta, utveckla samt säkerställa en störningsfri tillverkning. Vi ansvarar även för drift av renrum samt renmedia-anläggningar, och förvaltar ett flertal produktionsnära IT-system. Du kommer samarbeta med tekniker och processingenjörer för att hitta eventuella fel och nya lösningar.



I rollen som Automationsingenjör ingår arbetsuppgifter så som att:

* Driva förvaltning, underhåll och nyutveckling av automationssystem
* Medverka till att långsiktiga planer tas fram för automationssystem
* Underhålla, felsöka och uppdatera system med tillhörande dokumentation
* Medverka och driva avvikelseutredningar och ändringsärenden
* Medverka som Teknisk sakkunnig i projekt
* Medverka vid inspektioner och externa kontakter
* Initiera, driva och delta i förbättringsärenden
* Planera och genomföra tekniska försök samt delta i kvalificeringar



Är du den vi söker?

Vi söker dig som gillar att arbeta i ett team som ansvarar för drift, service och underhåll av automatiserade och datoriserade system. Du kommer vara en av fyra automationsingenjörer i teamet.



Du har förmodligen en högskoleingenjörsutbildning inom automation och några års erfarenhet av automation, programmering och underhåll, gärna inom liknande industri. Kompetens inom el, datorteknik, och nätverk är meriterande. Starkt meriterande anses tidigare erfarenhet från arbete inom serialisering.



Som person behöver du vara flexibel när det krävs. Vi hoppas att du vågar prova nya saker och utmanar sätter vi jobbat på. Du tycker om att ta egna initiativ och har ett brinnande intresse för teknik och problemlösning. Tjänsten kräver även att du har ett strukturerat arbetssätt för att upprätthålla en GxP miljö. Stor vikt kommer läggas vid dina personliga egenskaper.



Frågor och ansökan

På Galderma i Uppsala har vi verksamhet inom produktutveckling och tillverkning av världsledande produkter inom dermatologi och vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Vi är belägna längs med Fyrisån i Uppsala, 10 minuters cykelfärd från Uppsala Resecentrum.



Har vi fångat ditt intresse? Vi tar gärna emot din ansökan redan i dag, dock senast den 28/08 2025. Urval och intervjuer sker löpande under ansökningstiden. Visa mindre

About the role:

We are seeking an experienced Analytical Chemist to join our team and drive the development and validation of analytical methods for proteins. In this role, you'll work hands-on with techniques such as ELISA, SDS-PAGE, and Western Blot, while also supporting projects with expert advice and scientific reporting. If you're passionate about protein analysis, problem-solving, and collaborative science, we'd love to hear from you!



Your responsibilities will include:

*

Development of analytical methods for proteins, working procedures and documentation
* Analyses of explorative samples, mainly from Process Development
* Validation of analytical methods, laboratory analysis work and maintenance of instruments and equipment
* Participation in characterization of protein substances and formulations
* Acting as expert in appointed areas and supporting project teams with analytical testing competence
* Suggesting and developing new solutions to problems in order to improve performance
* Writing and reviewing scientific reports



Essential Qualifications

* Degree in biochemistry, analytical chemistry, or equivalent (PhD is preferred)
* 10+ years of experience working with proteins, including analytical testing, method development, and validation
* Hands-on experience with analytical methods such as ELISA, SDS-PAGE, Western Blot, IEF, and 2D-electrophoresis
* Skilled in writing scientific reports and/or regulatory documentation
* Fluency in English (Swedish fluency is preferred)



Essential Skills

* Strong analytical and problem-solving ability, with a drive to find new solutions
* Structured and organized, able to manage multiple tasks and deliver high-quality results on time
* Collaborative mindset: open, adaptable, and able to work effectively in cross-functional teams
* Confident communicator, able to present opinions in an open, honest, and constructive manner
* Strong delivery focus and ability to reliably achieve project goals



Desirable experience:

* Experience of working according to GMP is a merit



Selection is ongoing, so don't wait to submit your application! Visa mindre

Job Title: Process Development Engineer, Injectable Devices

Location: Uppsala, Sweden (Hybrid)



Job description :

We are looking for a new member to the Device injectables team within Manufacturing Science and Technology. The Process Development Engineer is a subject matter expert (SME) responsible for new product implementation (NPI) into a manufacturing facility, and for support of upstream processes during commercial manufacturing.



Key responsibilities:

*

Support new product implementation (NPI) strategy and all aspects of process validation, including process data reviews, investigations, risk management, and change implementation. Write validation documentation and execute process validation under guidance from senior scientists.
*

Serve as a technical SME representing MSAT in Technology Transfer projects.
*

Process owner to support day-to-day operations with a focus on continuous improvements. Identify opportunities for process enhancement, cost reduction, and efficiency gains, proactively driving necessary changes.
*

Lead and participate in investigations into deviations, incidents, and anomalies within the manufacturing process. Conduct in-depth root cause analysis to identify the underlying reasons for deviations and incidents, focusing on process improvement.
*

Collect data from various sources, including quality control reports, production logs, and other relevant documents, to support investigations and continuous process verification (CPV)
*

Write and review technical documentation ensuring compliance with regulatory and quality standards.
*

Coordinate with other experts and collaborate with cross-functional teams, including production, quality assurance, regulatory affairs, and process development, to ensure thorough investigation and timely issue resolution. Assist senior scientists in information gathering to support research studies and claims, and provide input to risk assessments/FMEAs.
*

Prepare detailed investigation reports, conveying findings and recommendations to management and relevant stakeholders





Skills & Qualifications

*

BSc or MSc degree in a relevant engineering field
*

Good familiarity with upstream manufacturing processes in the medical device and/or biopharmaceutical industry
*

1 to 3 years of experience in upstream operations, preferably in a biopharmaceutical/medical device manufacturing environment
*

Strong knowledge of investigative methodologies and root cause analysis techniques
*

Knowledge of regulatory requirements related to investigations and cGMP
*

Sterilization knowledge is meriting





What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



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 600 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.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Senior Sterilization Engineer

Location: Uppsala, Sweden (on-site, viss flexibilitet för distansarbete)



Job Description

Bli en del av Galdermas framgångsrika tillväxtresa - utvecklas i rollen som Senior Sterilization Engineer!



Vi söker en erfaren och engagerad Senior Sterilization Engineer till vårt team som arbetar med utveckling av nya injicerbara medical device. I den här rollen får du ett tekniskt ledaransvar inom sterilisering, ett av de mest avgörande områdena för patientsäkerheten. Därför söker vi dig som har djup kunskap och förståelse för steriliseringsprocessers komplexitet och betydelse. Som Senior Sterilization Engineer leder du arbetet med sterilitet och sterilisering av injicerbara produkter under utveckling. Du ansvarar för aktiviteter som sträcker sig genom hela utvecklingskedjan, från att ta fram nya steriliseringsprocesser till teknisk överföring och implementering i organisationen. Arbetet sker i linje med våra CMC- och produktutvecklingsplaner. Du bidrar även i regulatoriska ärenden, tar fram specifikationer och stöttar formuleringsarbetet.



Rollen är både tvärfunktionell och projektinriktad. Du samarbetar nära flera interna funktioner och fungerar som specialist i både operativa och strategiska frågeställningar. Uppdraget kombinerar teknisk expertis med praktiska och administrativa inslag och kräver därför god kommunikationsförmåga, stark samarbetsvilja och förmåga att arbeta självständigt.



Teamet består i dag av tio engagerade kollegor med fokus på utveckling av nya produkter och produktionsprocesser. Eftersom det för närvarande inte finns någon annan som arbetar specifikt med sterilisering blir du teamets främsta expert inom området. Du förväntas driva utvecklingen framåt på egen hand, men med stöd och expertis från andra delar av organisationen. Vi erbjuder en arbetsmiljö där inkludering, trivsel och samarbete står i fokus.



Ansvarsområden

* Leda och genomföra aktiviteter kopplade till sterilitet och steriliseringsprocesser för injicerbara produkter under utveckling, i enlighet med CMC-planer, projekt och program
* Utveckla nya och effektiva steriliseringsprocesser i linje med regulatoriska och kvalitetsmässiga krav
* Säkerställa smidig teknisk överföring av steriliseringsprocesser till relevanta delar av organisationen
* Bidra i regulatoriska inskick, designkontroll, specifikationer och formulering inom ramen för projekt
* Säkerställa att steriliseringsaktiviteter sker i enlighet med strategier, planer samt gällande regulatoriska krav, Galdermas kvalitetssystem, EHS-krav och internationella standarder



Kvalifikationer:

* En mikrobiologisk, maskinteknisk eller annan relevant teknisk eller naturvetenskaplig utbildning
* Djupgående kunskap om steriliseringsprocesser, dess metoder och komplexitet
* Dokumenterad erfarenhet av att arbeta i projektform, gärna i tvärfunktionella team
* Vana vid att verka inom branscher med högt ställda regulatoriska krav
* Erfarenhet av arbete med medicintekniska produkter (Medical Device)



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.

Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss i moderna lokaler utmed vackra Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag. Urval och intervjuer görs löpande.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren
* Nästa steg är en intervju med anställande chef samt ytterligare en chef från verksamheten
* Det sista steget i rekryteringsprocessen innebär att vi genomför referenstagningar



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Do you have deep experience in aseptic manufacturing and visual inspection systems? Are you comfortable stepping in as a subject matter expert when complex technical challenges arise? Galderma is now hiring a Senior Process Engineer with a focus on Aseptic Filling & Visual Inspection to support our continued growth and expansion.



About the role



As Senior Process Engineer, you will work as a subject matter expert (SME) in aseptic filling and visual inspection systems for both pre-filled syringes and vials. You'll play a key role in technical projects, equipment qualification, and process development. The role requires both hands-on expertise and strong collaboration across functions such as Production Engineering, Maintenance, Automation, and Quality.

You'll contribute to the evolution of our filling and inspection capabilities by supporting investigations, leading or participating in projects, and ensuring that systems and equipment are compliant, efficient, and fit for purpose.



Key responsibilities include:

* Lead and contribute to engineering projects related to aseptic filling and visual inspection of pre-filled syringes and vials
* Act as technical owner for filling and inspection equipment and associated specifications
* Provide technical input in deviation handling and root cause investigations
* Support design, procurement, and qualification of new or modified systems
* Collaborate across departments to support manufacturing improvements and regulatory compliance



What we're looking for



You have a university degree in engineering or equivalent practical experience and bring 10+ years of experience from pharmaceutical manufacturing environments. Your expertise lies in aseptic filling and visual inspection, with a solid understanding of Grade A cleanroom standards and cGMP compliance.

You're analytical, detail-oriented, and confident in handling technical investigations and process improvements. You collaborate well across teams, communicate clearly, and take initiative when challenges arise. Fluency in English is required. Apart from this we would appreciate if you bring the following:

* Experience with CAPEX projects related to filling or inspection equipment
* Involvement in equipment commissioning and qualification
* Familiarity with Part 11 compliance and automated systems
* Experience working with external equipment suppliers
* Swedish language skills



Why Galderma?



Galderma is in a period of significant growth, investing in new manufacturing capabilities and expanding internal production. That means the work goes beyond maintaining existing systems - there's a strong focus on designing, implementing, and improving new manufacturing lines and equipment.

The engineering work is technically demanding, involving aseptic manufacturing, cleanroom environments, and compliance with pharmaceutical and medical device regulations. It requires a high level of precision and problem-solving ability.

This position offers variety: no two days look the same and the process engineer is called upon when there are complex problems to solve, new equipment to bring in, or processes to improve. Visa mindre

Senior Filling Engineer

Location: Uppsala, Sweden (on-site, viss flexibilitet för distansarbete)



Job Description

Bli en del av Galdermas framgångsrika tillväxtresa - utvecklas i rollen som Senior Sterilization Engineer!



Vi söker en erfaren och engagerad Senior Filling Engineer till vårt team som arbetar med utveckling av nya injicerbara medical device. I denna roll får du ett tekniskt ledaransvar inom fyllning av injicerbara produkter. Du kommer att leda och genomföra aktiviteter kopplade till fyllningsprocesser inom ramen för våra utvecklingsprogram och CMC-planer. Arbetet omfattar bland annat regulatoriskt stöd, arbete med designkontroll, specifikationer samt stöd till formuleringsteamet. Rollen innebär ett nära samarbete med både interna och externa parter och sträcker sig över hela utvecklingskedjan, från processutveckling till överföring och implementering i den operativa organisationen.



Rollen är både tvärfunktionell och projektinriktad. Du samarbetar nära flera interna funktioner och fungerar som specialist i både operativa och strategiska projektmöten. Uppdraget kombinerar teknisk expertis med praktiska och administrativa inslag och kräver därför god kommunikationsförmåga, stark samarbetsvilja och förmåga att arbeta självständigt.



Teamet består i dag av tio engagerade kollegor med fokus på utveckling av nya produkter och produktionsprocesser.. Eftersom det för närvarande inte finns någon annan som arbetar specifikt med fyllning av injicerbara produkter blir du teamets främsta expert inom området. Du förväntas driva utvecklingen framåt på egen hand, men med stöd och expertis från andra delar av organisationen. Vi erbjuder en arbetsmiljö där inkludering, trivsel och samarbete står i fokus.



Ansvarsområden

* Leda och genomföra aktiviteter kopplade till fyllningsprocesser för injicerbara produkter under utveckling, i enlighet med fastställda CMC-planer, projekt och program
* Utveckla robusta och regulatoriskt godkända fyllningsprocesser
* Säkerställa effektiv teknisk överföring av fyllningsprocesser till relevanta delar av organisationen
* Bidra med tekniskt expertstöd i frågor kopplade till inskick till myndigheter, designkontroll, specifikationer och formulering
* Säkerställa att fyllningsaktiviteter följer uppsatt strategi och plan samt sker i enlighet med gällande regulatoriska krav, Galdermas kvalitetssystem och internationella standarder



Kvalifikationer:

* En bakgrund som maskiningenjör, kemiingenjör eller motsvarande relevant utbildning och erfarenhet
* Erfarenhet av att arbeta med fyllning av sterila läkemedel eller medicintekniska produkter (Medical Devices)
* God förståelse för krav på sterila processer och förpackningsintegritet, till exempel för sprutor eller liknande produkter
* Kunskap om produktionsutrustning och tekniska processer kopplade till tillverkning av sterila produkter
* Förmåga att arbeta strukturerat i en reglerad miljö med högt ställda krav på kvalitet och säkerhet



Vi erbjuder

Du kommer att arbeta för en organisation som innefattar mångfald och inkludering och vi tror att vi kommer att leverera bättre resultat genom att spegla perspektiven hos vår mångfaldiga kundbas.

I Uppsala ligger Galdermas globala center för affärsområdet estetik med verksamhet inom produktutveckling, tillverkning och marknadsföring. Här arbetar cirka 600 personer med världsledande produkter som Restylane, Azzalure och Sculptra.

Vi erbjuder dig möjligheten att arbeta i en spännande, internationell miljö där både personlig och professionell utveckling uppmuntras. Hos oss blir du en viktig del av ett globalt och växande företag. Du hittar oss i moderna lokaler utmed vackra Fyrisån, endast 10 minuters cykelväg från Uppsala Centralstation.



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag. Urval och intervjuer görs löpande.

* Om din profil är en matchning kommer vi bjuda in dig till ett första samtal med rekryteraren
* Nästa steg är en intervju med anställande chef samt ytterligare en chef från verksamheten
* Det sista steget i rekryteringsprocessen innebär att vi genomför referenstagningar



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Job Title: Utilities Engineer

Location: Uppsala



Galderma Uppsala is looking for a Utilities Engineer. The Utilities Engineer ensures that the site's utility systems are managed, maintained, and performs according to Galderma specifications and regulatory demands within medical device and pharmaceuticals.

The Utilities Engineer will manage WFI (Water For Injection), PW (Purified Water), Clean Steam, Clean Compressed Air and Process Gases, Cooling Water, Plant steam, and Compressed Air systems and more used in Galderma's production. He/she is responsible for planning routine testing and maintenance program for the site utility systems. Work will be done in close collaboration with utility technicians, production team, Quality Control as well as project engineers and provide guidance when needed.



Key Tasks

* Monitor and manage the operation of utility systems, ensuring performance. Plan and undertake ongoing maintenance, monitoring and troubleshooting of utility systems.
* Report, investigate and close deviations, execute CAPAs and Effectiveness checks within area of responsibility in accordance with Galderma Quality Management System.
* Involved in the planning and implementation of system upgrades or expansions to meet the changing needs of production.
* Ensure that utility systems comply with regulations and maintain accurate documentation, conduct audits prepare reports and participate in regulatory inspections
* Develop contingency plans and strategies to address utility related emergencies to ensure minimal downtime and business continuity
* Work with the various departments and teams within the manufacturing plant



Skills & Qualifications

* Engineering Degree or equivalent career experience
* Works with utilities in pharma/medical devices industry preferred but can also consider candidates working with similar job tasks with in other industries
* Knowledge of Good Manufacturing Practice
* Professional level Swedish and English is necessary as reports are in both Swedish and English
* Practical experience with Good Manufacturing Practice (GMP), and Deviations and CAPA
* Experience with ERP systems (e.g. SAP, M3) a plus



What we offer in return

You will be working with a highly experienced and innovative team involved in maintaining and improving current systems. In addition, the planned plant expansion means that there is an opportunity to participate in the design and installation of completely new utilities systems.

You will be working with a global dermatology company with operations in 90 countries. The Uppsala site is also Galderma's global centre for our aesthetics business and has operations in product development, manufacturing and marketing. We offer an opportunity to work in a dynamic and international environment where personal and professional development is encouraged. We are located along the river Fyrisån, 10 minutes by bike from Uppsala Central Station.'



Next Steps

We welcome your application via our company website: CAREERS | Galderma. If you are already employed at Galderma, please apply through our internal career site in Workday.

Submit your application as soon as possible, but no later than August 20, 2025. Please note that the selection process is ongoing and the position may be filled before the application deadline.

* If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
* The second stage involves an interview with the hiring manager and potentially a hiring manager colleague (on-site).
* The third stage includes an interview with the immediate team member, with hiring manager possibly joining for a brief portion of the meeting (on-site).
* Finally, reference checks and security screening will be conducted as part of the concluding process.



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Job Title: Senior DP-filling Scientist
Location: Uppsala, Sweden (onsite)



Join Our Mission to Advance Biologic Drug Development - We're Hiring a Senior DP-filling Scientist



Do you want to work hands-on with the development of high-quality biological Drug Products in an innovative and science-driven environment? Are you experienced in pharmaceutical manufacturing with specific skills and knowledge in DP-filling science such as formulation, sterile filtration and filling technology for biological products with a deep understanding of all requirements around aseptic filling and ready to shape future processes that bring biologic therapies to patients?



We are currently seeking a skilled and motivated Senior DP-filling Scientist to join our expanding team. In this role, you will contribute to the development and optimization of injectable drug product processes, with a clear focus on quality, scalability, and compliance.



What You Will Do



You will be part of the Product Science & MS&T function, supporting both early and late-stage development. Your key responsibilities will include:

· Designing and optimizing processes for formulation, filtration, and filling of drug products

· Translating development work into scalable, robust manufacturing processes

· Contributing to technology transfer, troubleshooting, and process improvements

· Supporting documentation for regulatory submissions and internal quality systems

· Collaborating closely with R&D, Operations, QA, and Regulatory Affairs



What You Bring



· A Master's or Bachelor's degree in Bioprocess Engineering, Chemical Engineering, Mechanical Engineering, or a related life science field

· At least 5 years of experience, 10-15 years is meriting, in drug product development, pharmaceutical process development, or related manufacturing roles

· Strong knowledge of formulation, mixing, and drug product handling

· Experience with aseptic processing, injectable products, or biologics is highly valued but not required



Soft Skills That Matter



· You are a strong communicator with the ability to work cross-functionally and build effective relationships

· You work in a structured, analytical way and take initiative to solve problems

· You are adaptable, collaborative, and motivated by quality and continuous improvement



Why Join Us?



· Be part of a growing organization focused on innovation in biologics and injectable drug products

· Join a passionate, skilled team with strong scientific expertise and collaborative culture

· Work from our expanding site in Uppsala, with career development opportunities and modern technology platforms

Ready to take the next step in your pharmaceutical career? Apply now and help us shape the future of injectable biologics. Visa mindre

Job Title: Process Development engineer, Assembly & Packaging

Location: Uppsala, Sweden (Hybrid)



Job description :

We are looking for a new member to the Assembly and Packaging team within Manufacturing Science and Technology. The Process Development engineer is a subject matter expert (SME) responsible for new product implementation (NPI) into a manufacturing facility, and for support of assembly and packaging processes during commercial manufacturing.



Key responsibilities:

*

Support new product implementation (NPI) strategy and all aspects of process validation, including process data reviews, investigations, risk management, and change implementation. Write validation documentation and execute process validation under guidance from senior scientists.
*

Serve as a technical SME representing MSAT in Technology Transfer projects.
*

Process owner to support day-to-day operations with a focus on continuous improvements. Identify opportunities for process enhancement, cost reduction, and efficiency gains, proactively driving necessary changes.
*

Lead and participate in investigations into deviations, incidents, and anomalies within the manufacturing process. Conduct in-depth root cause analysis to identify the underlying reasons for deviations and incidents, focusing on process improvement.
*

Collect data from various sources, including quality control reports, production logs, and other relevant documents, to support investigations and continuous process verification (CPV)
*

Write and review technical documentation ensuring compliance with regulatory and quality standards.
*

Coordinate with other experts and collaborate with cross-functional teams, including production, quality assurance, regulatory affairs, and process development, to ensure thorough investigation and timely issue resolution. Assist senior scientists in information gathering to support research studies and claims, and provide input to risk assessments/FMEAs.
*

Prepare detailed investigation reports, conveying findings and recommendations to management and relevant stakeholders





Skills & Qualifications

*

BSc or MSc degree in a relevant engineering field
*

Relevant operational experience from the industry
*

Experience of working with the transfer process from development to production/operations, or experience from a similar position.
*

Good familiarity with downstream manufacturing processes in the medical device and/or biopharmaceutical industry
*

1 to 3 years of experience in assembly and packaging operations, preferably in a biopharmaceutical/medical device manufacturing environment
*

Strong knowledge of investigative methodologies and root cause analysis techniques
*

Knowledge of regulatory requirements related to investigations and cGMP
*

Experience in technical writing



What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



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 600 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.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

* If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
* The next step is an interview with the hiring manager
* The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre

Job Title: Process Development Engineer, Injectable Devices

Location: Uppsala, Sweden (Hybrid)



Job description :

We are looking for a new member to the Device injectables team within Manufacturing Science and Technology. The Process Development Engineer is a subject matter expert (SME) responsible for new product implementation (NPI) into a manufacturing facility, and for support of upstream processes during commercial manufacturing.



Key responsibilities:

*

Support new product implementation (NPI) strategy and all aspects of process validation, including process data reviews, investigations, risk management, and change implementation. Write validation documentation and execute process validation under guidance from senior scientists.
*

Serve as a technical SME representing MSAT in Technology Transfer projects.
*

Process owner to support day-to-day operations with a focus on continuous improvements. Identify opportunities for process enhancement, cost reduction, and efficiency gains, proactively driving necessary changes.
*

Lead and participate in investigations into deviations, incidents, and anomalies within the manufacturing process. Conduct in-depth root cause analysis to identify the underlying reasons for deviations and incidents, focusing on process improvement.
*

Collect data from various sources, including quality control reports, production logs, and other relevant documents, to support investigations and continuous process verification (CPV)
*

Write and review technical documentation ensuring compliance with regulatory and quality standards.
*

Coordinate with other experts and collaborate with cross-functional teams, including production, quality assurance, regulatory affairs, and process development, to ensure thorough investigation and timely issue resolution. Assist senior scientists in information gathering to support research studies and claims, and provide input to risk assessments/FMEAs.
*

Prepare detailed investigation reports, conveying findings and recommendations to management and relevant stakeholders





Skills & Qualifications

*

BSc or MSc degree in a relevant engineering field
*

Good familiarity with upstream manufacturing processes in the medical device and/or biopharmaceutical industry
*

1 to 3 years of experience in upstream operations, preferably in a biopharmaceutical/medical device manufacturing environment
*

Strong knowledge of investigative methodologies and root cause analysis techniques
*

Knowledge of regulatory requirements related to investigations and cGMP
*

Sterilization knowledge is meriting





What we offer in return

You will be working for an organisation that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.



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 600 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.



Next steps

We welcome your application via our company website CAREERS | Galderma. Apply as soon as possible, as the selection process is ongoing continuously.

*

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
*

The next step is an interview with the hiring manager
*

The final step is a panel conversation with the extended team



Our people make a difference

At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. Visa mindre