Uppsala: Operator (Aseptics)

Hitta ansökningsinfo om jobbet Operator (Aseptics) i Uppsala. Är det intressant kan du gå vidare och ansöka jobbet. Annars kan du klicka på arbetsgivaren eller yrkesbenämningen för att se alla jobb i Uppsala inom den kategorin.

Publicerad: 2025-06-16 // Varaktighet: Heltid

Operatör (Aseptisk fyllning) med inriktning granskning av tillverkningsdokumentation

Location: Uppsala (on-site, skiftgång)



Job Description

Nu har du möjlighet att bli en del av Galdermas tillväxtresa och utvecklas i rollen som 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 läkemedelsprodukt Relfydess. Inledningsvis kommer tjänsten fokusera på granskning av tillverkningsdokumentation.

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. Tjänsten kommer fokusera på granskning av batchdokumentation och du kommer ansvara för att batchdokumentationen är komplett inom satta tidsramar.



I tjänsten kommer du att:

* Granska tillverkningsdokumentation så som batchprotokoll med dess bilagor, trendfiler och instruktioner.
* 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:

* Erfarenhet av aseptiskt operatörsarbete
* Erfarenhet av granskning av batchdokumentation.
* 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

I tjänsten kommer skiftarbete att ingå.



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.

* 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 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.

Alla platsannonser →

Andra jobb i Uppsala som Processoperatör, kemisk industri

Nedan visas andra jobb i Uppsala som Processoperatör, kemisk industri.

Processoperatör inom läkemedelsproduktion för framtida uppdrag i Uppsala

Läs mer Jul 16
Academic Resource söker Processoperatörer inom läkemedelsproduktion för framtida konsultuppdrag till Life Science företag i Uppsala.
Start enligt överenskommelse.
Arbetstiderna är dagtid.


Kvalifikationer:
Vi söker dig som har erfarenhet av tillverkning-/processarbete från läkemedelsindustri eller likvärdigt.
Det anses som meriterande med erfarenhet från process-eller produktionsarbete från andra branscher än läkemedelsindustrin.
Kunskaper om GMP är meriterande.


Personliga egenskaper som värdesätts är noggrannhet, förmåga att kunna arbeta självständigt, flexibilitet, stresstålighet och god samarbetsförmåga.
För att klara av att utföra arbetsuppgifterna måste du tala, skriva och förstå både svenska och engelska obehindrat.


Arbetsuppgifter:
• Delta i det dagliga arbetet och i tillverkningsprocesser inom arbetsområdet.
• Följa instruktioner och metoder för tillverkning.
• Följa GMP- och myndighetskrav samt arbetsmiljöregler.
• Dokumentera egna utförda arbetsmoment.
• Rapportera avvikelser till arbetsledaren.


Ansökan:
Intervjuer och urval kommer att ske löpande, så skicka gärna din ansökan så snart som möjligt.
Klicka nedan på sök tjänsten och fyll i dina kontaktuppgifter, ange referensnamn: SOP0425

Ansök nu

Processoperatör

Läs mer Jun 30
Bli del av något större
Är du redo att ta din potential till nästa nivå och göra verklig skillnad inom Life Science, diagnostik och bioteknik?
På Cytiva, ett av Danahers 15 dotterbolag, räddar vårt arbete liv. Hos oss blir du del av en kultur som präglas av gemenskap och tillhörighet där ditt unika perspektiv spelar roll. Med hjälp av Danaher Business System omvandlar vi idéer till konkreta lösningar.?
Att arbeta på Cytiva innebär att ligga i framkant av att utveckla nya sätt att förbättra människors hälsa. Våra kunder bedriver allt från grundläggande biologisk forskning till att utveckla innovativa vacciner, nya läkemedel och cell- och genterapier.
På Cytiva får du chansen att utvecklas tillsammans med oss och göra verklig skillnad för människor världen över. Ta chansen att bli del av något större.
Läs mer om Danaher Business System som gör allt möjligt.
Vi söker en Processoperatör till sektionen Kolonnproduktionen på Cytivas site i Uppsala. Teamet på Kolonnproduktionen består av produktionsingejörer, processoperatörer och sektionschef som tillsammans arbetar med att tillverka och kvalitetstesta packade kolonner där operatörerna utför och ansvarar för alla moment i sin produktionsbatch. Sektionen tillverkar även kit, reservdelar och tomkolonner.
Tjänsten är en tillsvidareanställning. Arbetet är förlagt dagtid måndag-fredag på plats på Cytivas site i Uppsala.
Dina arbetsuppgifter:
Batchvis tillverkning, kvalitetskontroll och förpackning av slutprodukt enligt gällande metoder.
Dokumentera tillverkning och kvalitetstester enligt gällande metoder och avrapportera resultaten i gällande system.
Uppmärksamma, rapportera och felsöka vid kvalitetsproblem.
Delta i sektionens löpande förbättringsarbete.

De huvudsakliga kraven för tjänsten innefattar:
Gymnasial utbildning i kemi/naturkunskap/maskinteknik, alternativt eftergymnasial operatörsutbildning eller motsvarande arbetslivserfarenhet från produktion-/processindustri.
Erfarenhet/utbildning i hantering av kemikalier och brandfarliga varor.
God system- och datorvana.
Behärskar svenska språket i tal och skrift samt grundläggande kunskaper i engelska.

Det är meriterande om du även har:
Erfarenhet av att driva förbättringsarbeten i produktionsmiljö.
Kunskap om Cytivas produkter och tillverkningsprocesser.

Vi ser gärna att du som söker är en kvalitetsmedveten och noggrann person med god samarbetsförmåga. För att vara framgångsrik i rollen är det även viktigt att du som person är flexibel, ansvarstagande, engagerad i ditt arbete.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag.

Ansök nu

Processoperatör, Pilot Plant

Läs mer Maj 16
Bli del av något större
Är du redo att ta din potential till nästa nivå och göra verklig skillnad inom Life Science, diagnostik och bioteknik??
På Cytiva, ett av Danahers 15 dotterbolag, räddar vårt arbete liv. Hos oss blir du del av en kultur som präglas av gemenskap och tillhörighet där ditt unika perspektiv spelar roll. Med hjälp av Danaher Business System omvandlar vi idéer till konkreta lösningar.?
Att arbeta på Cytiva innebär att ligga i framkant av att utveckla nya sätt att förbättra människors hälsa. Våra kunder bedriver allt från grundläggande biologisk forskning till att utveckla innovativa vacciner, nya läkemedel och cell- och genterapier.
På Cytiva får du chansen att utvecklas tillsammans med oss och göra verklig skillnad för människor världen över. Ta chansen att bli del av något större.
Läs mer om Danaher Business System som gör allt möjligt.
Vi söker en Processoperatör till sektionen Pilot Plant & V1 Dry Filling på Cytivas site i Uppsala. Teamet på Pilot Plant består av underhållsoperatör, sektionschef och tre produktionsoperatörer som tillsammans arbetar med att producera separationsmedia som används av våra kunder för att analysera proteiner i diverse forsknings och läkemedelsapplikationer. Del av tillverkningen på Pilot Plant är automatiserad där styrsystem Sattline och batchprotokoll används dagligen.
Tjänsten är en tidsbegränsad anställning som sträcker sig fram till 31 december 2025. Arbetet är förlagt dagtid måndag-fredag på plats på Cytivas site i Uppsala.
Dina arbetsuppgifter:
Tillverka sektionens produktsortiment i enlighet med gällande metoder, rutiner och instruktioner.
Uppmärksamma och rapportera kvalitetsavvikelser samt dokumentera kvalitetsdata.
Aktivt medverka i sektionens arbete kring ständiga förbättringar.

De huvudsakliga kraven för tjänsten innefattar:
Gymnasial utbildning i kemi/naturkunskap/maskinteknik, alternativt eftergymnasial operatörsutbildning eller motsvarande arbetslivserfarenhet från produktion-/processindustri.
Erfarenhet/utbildning i hantering av kemikalier och brandfarliga varor.
God system- och datorvana.
Behärskar svenska språket i tal och skrift samt grundläggande kunskaper i engelska.

Det är meriterande om du även har:
Erfarenhet av att driva förbättringsarbeten i produktionsmiljö.
Kunskap om Cytivas produkter och tillverkningsprocesser.

Vi ser gärna att du som söker är en kvalitetsmedveten och noggrann person med god samarbetsförmåga. För att vara framgångsrik i rollen är det även viktigt att du som person är flexibel, ansvarstagande, engagerad i ditt arbete.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande den här tjänsten vänligen kontakta Emil Larsson, emil.larsson@cytiva.com. Välkommen med din ansökan!

Ansök nu

Processoperatör, Kolonnproduktion

Läs mer Maj 23
Bli del av något större
Är du redo att ta din potential till nästa nivå och göra verklig skillnad inom Life Science, diagnostik och bioteknik?
På Cytiva, ett av Danahers 15 dotterbolag, räddar vårt arbete liv. Hos oss blir du del av en kultur som präglas av gemenskap och tillhörighet där ditt unika perspektiv spelar roll. Med hjälp av Danaher Business System omvandlar vi idéer till konkreta lösningar.?
Att arbeta på Cytiva innebär att ligga i framkant av att utveckla nya sätt att förbättra människors hälsa. Våra kunder bedriver allt från grundläggande biologisk forskning till att utveckla innovativa vacciner, nya läkemedel och cell- och genterapier.
På Cytiva får du chansen att utvecklas tillsammans med oss och göra verklig skillnad för människor världen över. Ta chansen att bli del av något större.
Läs mer om Danaher Business System som gör allt möjligt.
Vi söker en Processoperatör till sektionen Kolonnproduktionen på Cytivas site i Uppsala. Teamet på Kolonnproduktionen består av produktionsingejörer, processoperatörer och sektionschef som tillsammans arbetar med att tillverka och kvalitetstesta packade kolonner där operatörerna utför och ansvarar för alla moment i sin produktionsbatch. Sektionen tillverkar även kit, reservdelar och tomkolonner.
Tjänsten är en tillsvidareanställning. Arbetet är förlagt dagtid måndag-fredag på plats på Cytivas site i Uppsala.
Dina arbetsuppgifter:
Batchvis tillverkning, kvalitetskontroll och förpackning av slutprodukt enligt gällande metoder.
Dokumentera tillverkning och kvalitetstester enligt gällande metoder och avrapportera resultaten i gällande system.
Uppmärksamma, rapportera och felsöka vid kvalitetsproblem.
Delta i sektionens löpande förbättringsarbete.

De huvudsakliga kraven för tjänsten innefattar:
Gymnasial utbildning i kemi/naturkunskap/maskinteknik, alternativt eftergymnasial operatörsutbildning eller motsvarande arbetslivserfarenhet från produktion-/processindustri.
Erfarenhet/utbildning i hantering av kemikalier och brandfarliga varor.
God system- och datorvana.
Behärskar svenska språket i tal och skrift samt grundläggande kunskaper i engelska.

Det är meriterande om du även har:
Erfarenhet av att driva förbättringsarbeten i produktionsmiljö.
Kunskap om Cytivas produkter och tillverkningsprocesser.

Vi ser gärna att du som söker är en kvalitetsmedveten och noggrann person med god samarbetsförmåga. För att vara framgångsrik i rollen är det även viktigt att du som person är flexibel, ansvarstagande, engagerad i ditt arbete.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande den här tjänsten vänligen kontakta Martina Brolin på martina.brolin@cytiva.com. Varmt välkommen med din ansökan!

Ansök nu

Andra jobb i Uppsala från Q-Med AB

Nedan visas andra jobb i Uppsala från Q-Med AB .

Manager MSAT Device Injectables

Civilingenjör, process, kemiteknik
Läs mer Jul 17
Nytt
Job Title: Manager MSAT Device Injectables

Location: Uppsala, Sweden (Hybrid)



Job description :

*

In this role, you will manage a team of Device Injectables manufacturing scientists responsible for new product implementation (NPI) into a manufacturing facility and for support of assembly and packaging processes during commercial manufacturing. You and your team will demonstrate a strong process ownership by turning technologies into manufacturing capabilities by applied science and technical investigations, ensuring continuous process improvements through consistent methodology.



Key responsibilities:



You and your team are responsible for:

*

Implementing plans and programs and support policies and practices related to the end-to-end manufacturing processes of NPI projects at all stages, from prototyping to final stage
*

Enabling smooth transition of products from R&D into full production readiness, with team members representing MSAT in Technology Transfer projects and taking full process ownership
*

Ensuring suggested design made by engineering optimizes the production process in terms of process efficiency, cycle time, reliability, and serviceability
*

Process material for commercial production
*

Identifying and implementing bulk and filling manufacturing processes for existing device injectable products
*

Process validation (PV), process trending programs, and continuous process verification (CPV) where applicable
*

Supplying technical manufacturing process expertise for appointed areas supporting daily operations, projects, regulatory applications, and audit presentations
*

Owning change controls within appointed area
*

Assessment and implementation of regulatory requirements according to List of Regulatory Requirements (LoRR)
*

Ownership for process material specifications for commercial production and product specifications
*

Ownership for E2E manufacturing processes including process risk assessments and post validation process descriptions
*

Ownership for medical device design control documentation following product design transfer



As Manager MSAT Device Injectables, you will have extensive contact with other departments and external parties, and are expected foster cooperation and partnership to provide integrated solutions to problems. You will guide key stakeholders on processes, systems and tools, and are to develop strong, trusting cross-functional relationships with senior business leaders




Skills & Qualifications

*

BSc or MSc degree in a relevant scientific or engineering field, such as Chemistry, Biochemistry, Chemical Engineering, or solid experience of working in a regulated industrial environment
*

Minimum of 8 years of experience with injectables in a biopharmaceutical and/or medical device environment
*

Previous team management experience
*

Fluent in English and Swedish





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 the selection process is ongoing.

*

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.

Ansök nu

Process Development Engineer, Biologics

Biomedicinare
Läs mer Jul 17
Nytt
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.

Ansök nu

Manager MSAT Assembly & Packaging

Civilingenjör, produktion, maskin
Läs mer Jul 17
Nytt
Job Title: Manager MSAT Assembly & Packaging

Location: Uppsala, Sweden (Hybrid)



Job description :

*

In this role, you will manage a team of Assembly & Packaging manufacturing scientists responsible for new product implementation (NPI) into a manufacturing facility and for support of assembly and packaging processes during commercial manufacturing.
*

You and your team will demonstrate a strong process ownership by turning technologies into manufacturing capabilities by applied science and technical investigations, ensuring continuous process improvements through consistent methodology.



Key responsibilities:

You and your team are responsible for:

*

Implementing plans and programs and support policies and practices related to the end-to-end manufacturing processes of NPI projects at all stages, from prototyping to final stage
*

Enabling smooth transition of products from R&D into full production readiness, with team members representing MSAT in Technology Transfer projects and taking full process ownership
*

Ensuring suggested design made by engineering optimizes the production process in terms of process efficiency, cycle time, reliability, and serviceability
*

Process material for commercial production
*

Identifying and implementing assembly and packaging manufacturing processes for existing biologic and device injectable products
*

Process validation (PV), process trending programs, and continuous process verification (CPV) where applicable
*

Supplying technical manufacturing process expertise for appointed areas supporting daily operations, projects, regulatory applications, and audit presentations
*

Owning change controls within appointed area
*

Assessment and implementation of regulatory requirements according to List of Regulatory Requirements (LoRR)



As Manager MSAT T Assembly & Packaging, you will have extensive contact with other departments and external parties, and are expected foster cooperation and partnership to provide integrated solutions to problems. You will guide key stakeholders on processes, systems and tools, and are to develop strong, trusting cross-functional relationships with senior business leaders



Skills & Qualifications

*

BSc or MSc degree in a relevant engineering field and/or working experience in an industrial environment
*

Minimum of 8 years of experience in a biopharmaceutical/medical device or other regulated environment
*

Previous team management experience
*

Hands on experience with manufacturing processes, control strategies and product interactions in the medical device and/or biopharmaceutical industry.
*

Fluent in English and Swedish





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.

Ansök nu

Process Development engineer, Assembly & Packaging

Civilingenjör, produktion, maskin
Läs mer Jul 17
Nytt
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.

Ansök nu

Process Development Engineer, Injectable Devices

Civilingenjör, process, kemiteknik
Läs mer Jul 17
Nytt
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.

Ansök nu

Senior Analytical Scientist

Analytisk kemist
Läs mer Jul 4
Job Title: Sr Analytical Scientist

Location: Uppsala, Sweden, On-site



Job Description

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

The Analytical Development-Chemistry team, a part of the Injectable Aesthetics Development department in Uppsala, is responsible for developing new products to further expand Galderma´s portfolio. To this positive and engaged group we are now looking for a Senior Analytical Scientist.



About the role

As Sr Analytical Chemist, 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 analytical 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 analytical 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 analytical chemistry (either PhD or similar experience) and additional experience from working in the medical device or pharmaceutical industry.

We think that you have the following skills and competences:

* Proficiency within advanced analytical chemistry (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.



Preferred qualifications include:

* Experience from Design Control is a merit
* Experience from E&L studies is a merit
* High level of statistical analysis skills 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
* A diverse park of analytical instruments including NMR, GC-MS, UHPLC-MS, ICP-MS, SEC-MALS, SEM, DSC, Raman, IR, NIR, rheometers and more
* Competitive salary and benefits.
* A collaborative and inclusive work culture.
* A chance to contribute to the global success of Galderma.



Your application

You are welcome to send your application in English or Swedish as soon as possible though no later than 2025-08-15 to Frida Wende. Should you have questions about this opportunity you are welcome to contact recruiting manager Frida Wende (Manager Analytical Development - Chemistry) on phone number 076-898 11 39.



Next Step
Have we caught your interest? We welcome your application via the "Apply Now" link as soon as possible, but no later than August 15, 2025. Selection and interviews will be conducted on an ongoing basis during the application period and the position may be filled before the final application date. . Should you have questions about this opportunity you are welcome to contact recruiting manager Frida Wende (Manager Analytical Development - Chemistry) on phone number 076-898 11 39.

* If your profile matches the requirements, you will be invited to an initial conversation with the recruiter.
* This will be followed by an interview with the hiring manager and a peer manager
* The final step in the process will be the completion of reference checks



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



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.

Ansök nu