Biolog - Lediga jobb

Arbetsbeskrivning

Redo för nästa steg i labbet? Randstad söker mikrobiologer för framtida konsultuppdrag!

Har du hunnit samla på dig värdefull erfarenhet av mikrobiologiskt arbete och känner att det börjar bli dags för nya utmaningar? Inom Life Science-sektorn händer det mycket just nu, och vi på Randstad Life Sciences ser en ständigt hög efterfrågan på skickliga mikrobiologer hos våra spännande kunder.

Därför jobbar vi nu proaktivt för att knyta kontakt med dig som vill ligga steget före. Genom att skicka in en spontanansökan till oss ser vi till att matcha din unika kompetens med rätt företag och konsultuppdrag så fort din nästa drömroll dyker upp.

Vem letar vi efter?

Vi söker dig som är trygg i din profession och trivs i en kvalitetsfokuserad laboratoriemiljö. Du är ambitiös, ansvarsfull och van vid att arbeta metodiskt.

Vi ser gärna att du har:

• En akademisk examen (Kandidat eller Master) inom mikrobiologi, infektionsbiologi, molekylärbiologi eller motsvarande.
• 1–5 års praktisk arbetslivserfarenhet från ett mikrobiologiskt laboratorium.
• God vana av metoder som bioburden, endotoxintestning (LAL/Kinetisk), miljö- och hygienkontroller, Total Viable Count (TVC) samt filtreringstekniker.
• Erfarenhet av att arbeta i en strikt reglerad miljö (exempelvis GMP, GLP eller ISO-standarder).
• Erfarenhet av arbete i renrum är starkt meriterande.

Vad innebär det att vara konsult hos Randstad?

Som konsult hos oss på Randstad Life Sciences får du det bästa av två världar – en trygg anställning hos oss och möjligheten att arbeta ute hos spännande kunder. Du får en dedikerad konsultchef som fungerar som din partner och ett bollplank i din karriärutveckling. Oavsett om du vill optimera processer, fördjupa dig inom kvalitetskontroll (QC) eller testa nya analysmetoder, ger konsultrollen dig en unik chans att bygga ett starkt nätverk och snabbt bredda ditt CV. Vi samarbetar med allt från innovativa startups till stora, globala läkemedelsbolag.

Låter det intressant?

Även om du inte söker nytt uppdrag exakt idag, vill vi gärna veta vem du är! Skicka gärna in ditt CV så hör vi av oss.

Ansvarsområden

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Kvalifikationer

• En akademisk examen (Kandidat eller Master) inom mikrobiologi, infektionsbiologi, molekylärbiologi eller motsvarande.
• 1–5 års praktisk arbetslivserfarenhet från ett mikrobiologiskt laboratorium.
• God vana av metoder som bioburden, endotoxintestning (LAL/Kinetisk), miljö- och hygienkontroller, Total Viable Count (TVC) samt filtreringstekniker.
• Erfarenhet av att arbeta i en strikt reglerad miljö (exempelvis GMP, GLP eller ISO-standarder).
• Erfarenhet av arbete i renrum är starkt meriterande.

Om företaget

Randstad

Med närmare 600 000 anställda i 38 länder är Randstad världsledande inom HR-tjänster, med målsättningen att bli världens främsta och mest uppskattade partner på arbetsmarknaden. Genom att kombinera vår passion för människor med kraften i dagens teknologi hjälper vi människor och företag att uppnå deras fulla potential. Vi kallar det Human Forward.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

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.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

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.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

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.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

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.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

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.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

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.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

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.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

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.

We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site.

You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation.

Key Responsibilities

• Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards.

• Oversee environmental monitoring, cleanroom qualification, and aseptic practices.

• Review sterilization validations and lead media fill programs.

• Drive contamination risk assessments, investigations, and CAPAs.

• Act as SME during audits and inspections.

• Provide training and mentorship in sterility assurance best practices.

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

You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift.

You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it.

Requirements

• Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline.

• 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry.

• Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits.

• Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations.

Skills

• Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control.

• Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems.

• Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S).

• Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies.

• Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives.

• Excellent documentation skills and a structured approach to problem-solving and investigations.

• Strong communication and collaboration skills with the ability to influence cross-functional teams.

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. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

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.