Civilingenjör inom bioteknik - Lediga jobb

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

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.

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 commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

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.

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 commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

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.

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 commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

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.

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 commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

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.

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 commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

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.

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 commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

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.

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 commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger.

You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements.

Key Responsibilities

• Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes.

• Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance.

• Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices.

• Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes.

• Design and evaluate smoke studies to verify airflow performance and first-air protection.

• Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies.

The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week.

You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment.

• Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations.

• Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing.

• Proven track record leading deviation investigations, root cause analyses, and CAPA implementation.

• Excellent analytical, problem-solving, and technical writing skills.

• Strong stakeholder management and collaboration across multiple functions.

• Ability to independently manage complex projects and drive continuous improvement initiatives.

If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application.

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.

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 commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

Därför är detta jobb för dig Du vill vara en del av regionens främsta Life Science-konsulter. Vi bidrar gemensamt med våra kunder till att förbättra människors liv och livskvalitet genom att bland annat utveckla produktion, kvalitet och projektverksamhet.

Här sätts du och din utveckling i fokus, du kommer ha en kontinuerlig dialog med din chef om utvecklingsmöjligheter framåt för att forma en plan och resa som passar dig och dina ambitioner. Som konsult på Knightec Group kommer du ha ett starkt stöd av ledare och dina kollegor där ni hjälper varandra att lyckas i uppdrag, projekt och i er utveckling.

Du blir en del av vårt affärsområde inom Compliance & Management där vi stöttar en effektiv omställning till digitala, hållbara och säkra lösningar genom expertkunskap inom exempelvis kvalitet, säkerhet, hållbarhet och projektstyrning.

Arbetsuppgifter Vårt team besitter en bred kunskap inom Life Science och dina uppdrag kommer att variera och kan innebära både roller i våra egna leveranser i interna team samt i våra kunders verksamheter. Du kommer arbeta inom något av nedan områden:

• validering/kvalificering

• projektledning

• processutveckling/produktionsutveckling

• QA IT

Kvalifikationer För att passa i rollen vill du arbeta i komplexa produktionsmiljöer, har en förmåga att arbeta förbättringsorienterat och gillar att ha olika kontaktytor. För att lyckas i rollen har du även:

• Nyfikenhet på/kännedom om konsultrollen

• Erfarenhet av arbete inom läkemedelsindustrin eller den medicintekniska branschen

• God kännedom om relevanta regelverk

• Relevant ingenjörsexamen eller motsvarande

• Flytande kunskaper i svenska och engelska, i tal och skrift 

En spännande resa med Knightec Group Knightec Group är idag en av Norra Europas ledande strategiska partners inom produkt- och digital tjänsteutveckling – hur häftigt är inte det?

Genom att förena ingenjörskompetens, digital expertis och affärsförståelse hjälper vi våra kunder att omvandla ny teknik till verkliga lösningar som skapar värde. Vi arbetar i skärningspunkten mellan affärsstrategi och teknikutveckling och stöttar våra kunder genom hela resan – från de första idéerna till utveckling, implementering och vidare utveckling.

På Knightec Group samlas människor med olika perspektiv, erfarenheter och specialistområden. Tillsammans skapar vi innovation som gör verklig skillnad – för företag, människor och samhället i stort.

För våra medarbetare innebär det stora möjligheter att vara med och forma framtidens lösningar genom meningsfulla projekt i teknikens absoluta framkant. Här får du inte bara utvecklas och växa i din roll – du blir också en del av ett team där nyfikenhet, samarbete och modet att utmana driver oss framåt.

Låter det som platsen för dig? Häng med på vår fortsatta resa!

Praktisk information Detta är en tjänst placerad på vårt kontor i Södertälje, Storgatan 41C. Resor i tjänsten kan förekomma till våra kunder. Startdatum är enligt överenskommelse.

Skicka in din ansökan så snart som möjligt, men senast 2026-09-30. Om du har några frågor om tjänsten är du välkommen att kontakta Kicki Björ, Talent Acquisition Specialist. Vi hanterar alla ansökningar via vår karriärsida för att säkerställa en trygg och säker hantering av dina personuppgifter i enlighet med GDPR.

Vi ser fram emot att höra från dig!

Därför är detta jobb för dig Du vill vara en del av regionens främsta Life Science-konsulter. Vi bidrar gemensamt med våra kunder till att förbättra människors liv och livskvalitet genom att bland annat utveckla produktion, kvalitet och projektverksamhet.

Här sätts du och din utveckling i fokus, du kommer ha en kontinuerlig dialog med din chef om utvecklingsmöjligheter framåt för att forma en plan och resa som passar dig och dina ambitioner. Som konsult på Knightec Group kommer du ha ett starkt stöd av ledare och dina kollegor där ni hjälper varandra att lyckas i uppdrag, projekt och i er utveckling.

Du blir en del av vårt affärsområde inom Compliance & Management där vi stöttar en effektiv omställning till digitala, hållbara och säkra lösningar genom expertkunskap inom exempelvis kvalitet, säkerhet, hållbarhet och projektstyrning.

Arbetsuppgifter Vårt team besitter en bred kunskap inom Life Science och dina uppdrag kommer att variera och kan innebära både roller i våra egna leveranser i interna team samt i våra kunders verksamheter. Du kommer arbeta inom något av nedan områden:

• validering/kvalificering

• projektledning

• processutveckling/produktionsutveckling

• QA

• QA IT

Kvalifikationer För att passa i rollen vill du arbeta i komplexa produktionsmiljöer, har en förmåga att arbeta förbättringsorienterat och gillar att ha olika kontaktytor. För att lyckas i rollen har du även:

• Nyfikenhet på/kännedom om konsultrollen

• Erfarenhet av arbete inom läkemedelsindustrin eller den medicintekniska branschen

• God kännedom om relevanta regelverk

• Relevant ingenjörsexamen eller motsvarande

• Flytande kunskaper i svenska och engelska, i tal och skrift 

En spännande resa med Knightec Group Knightec Group är idag en av Norra Europas ledande strategiska partners inom produkt- och digital tjänsteutveckling – hur häftigt är inte det?

Genom att förena ingenjörskompetens, digital expertis och affärsförståelse hjälper vi våra kunder att omvandla ny teknik till verkliga lösningar som skapar värde. Vi arbetar i skärningspunkten mellan affärsstrategi och teknikutveckling och stöttar våra kunder genom hela resan – från de första idéerna till utveckling, implementering och vidare utveckling.

På Knightec Group samlas människor med olika perspektiv, erfarenheter och specialistområden. Tillsammans skapar vi innovation som gör verklig skillnad – för företag, människor och samhället i stort.

För våra medarbetare innebär det stora möjligheter att vara med och forma framtidens lösningar genom meningsfulla projekt i teknikens absoluta framkant. Här får du inte bara utvecklas och växa i din roll – du blir också en del av ett team där nyfikenhet, samarbete och modet att utmana driver oss framåt.

Låter det som platsen för dig? Häng med på vår fortsatta resa!

Praktisk information Detta är en tillsvidareanställning med en provanställning på sex månader, placerad på något av våra kontor i Stockholm, Hagaesplanaden 49 (Forskaren) eller Rättarvägen 3 (Solna). Resor i tjänsten kan förekomma till våra kunder. Startdatum är enligt överenskommelse.

Skicka in din ansökan så snart som möjligt, men senast 2026-09-30. Om du har några frågor om tjänsten är du välkommen att kontakta Kicki Björ, Talent Acquisition Specialist. Vi hanterar alla ansökningar via vår karriärsida för att säkerställa en trygg och säker hantering av dina personuppgifter i enlighet med GDPR.

Vi ser fram emot att höra från dig!