Uppsala: Manufacturing Scientist, Assembly & Packaging

Hitta ansökningsinfo om jobbet Manufacturing Scientist, Assembly & Packaging 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: 2025-05-08 // Varaktighet: Heltid

Job Title: Manufacturing Scientist, 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 manufacturing scientist 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.

Alla platsannonser →

Andra jobb i Uppsala som Processingenjör, kemiteknik

Nedan visas andra jobb i Uppsala som Processingenjör, kemiteknik.

Processingenjör till Metacon

Läs mer Maj 16
Nytt
Metacons vision är att bli en ledande leverantör av system för lokal vätgasproduktion i Europa för industri- och transportsektorn. Vi tillhandahåller ledande teknologier och lösningar för produktion av grön vätgas – ett nyckelverktyg för omställningen till ren energi och fossilfri bränsleförsörjning

Vårt mål är att etablera oss som en av de marknadsledande aktörerna inom fossilfri grön vätgasproduktion för både transport- och industrisektorn. Vi engagerar oss för att fullt ut utnyttja vätgasens potential med målet att kraftigt minska växthusgasutsläpp och därmed bidra till att minska klimatförändringarna.

Drivs du av att göra skillnad och uppskattar att arbeta i en dynamisk, utvecklande och internationell miljö, omgiven av drivna, kompetenta och generösa kollegor – då är detta en roll för dig.

Arbetsuppgifter och ansvarsområden
Som processingenjör på Metacon är du en nyckelspelare för att skapa välfungerande tekniska plattformar.

Dina ansvarsområden inkluderar bland annat:

• Designa, utvärdera och optimera processer för produktion av drift av anläggningar, med fokus på säkerhet, effektivitet och hållbarhet
• Utföra processanalyser, inklusive termodynamiska beräkningar, flödesanalyser och felsökningar
• Ta fram och uppdatera tekniska specifikationer, processflödesscheman (PFD), rör- och instrumentdiagram (P&ID;) samt annan teknisk dokumentation
• Delta i projekt från designfas till driftsättning för att säkerställa att processlösningar är kostnadseffektiva och uppfyller krav
• Genomföra riskbedömningar (HAZOP) och delta i säkerhetsgranskningar
• Stötta projektledare och projektteam med teknisk expertis inom processfrågor
• Driva och dokumentera förbättringsprojekt för att optimera prestanda och minska kostnader
• Samverka med leverantörer, kunder och andra externa intressenter för att hitta bästa möjliga processlösningar

Profil

• Civil- eller högskoleingenjör inom kemiteknik, processteknik, energi eller liknande
• Minst 3-5 års erfarenhet av processdesign, optimering eller drift inom energi, industri eller gasprocesser
• Erfarenhet av arbete med processimulering
• God förståelse för regelverk inom industristandarder och säkerhet (t.ex. PED, ATEX mm)
• Erfarenhet av att stödja säljprocessen med tekniska analyser och lösningar är meriterande
• I tjänsten ingår en del resor, så B-körkort är ett krav
• Du talar och skriver bra på engelska

Vi söker dig som är van vid att arbeta tvärfunktionellt och har förmåga att ta ett helhetsgrepp över våra tekniska lösningar. Utöver processdesign kommer du att vara en nyckelperson i samverkan med automation, el och andra discipliner och fungera som teknisk ledare i utvecklings- och kundprojekt.

Vidare ser vi gärna att du kan agera teknisk lead i tvärdisciplinära projekt med ansvar för att samordna teknikval inom process, automation och el. Samt att du har god förståelse för angränsande discipliner såsom automation och el, du behöver inte vara expert men tillräckligt insatt för att kunna koordinera tekniska lösningar med specialister

För att passa och trivas i rollen tror vi att du är analytisk och lösningsorienterad samt har ett strukturerat arbetssätt. Du är kommunikativ och skicklig på att samarbeta med olika funktioner och intressenter. Vidare tror vi att du är innovativ och nyfiken med en stark vilja att driva förbättringsarbete.

Inom Metacon förväntas en hög grad av samarbete och kollegialt lärande och därför värdesätts både din tekniska och din sociala kompetens samt din samarbetsförmåga och nyfikenhet för teknik. Du drivs av att hitta de bästa lösningarna så att bolagets kunder blir nöjda. Metacon söker dig som vill vara med och påverka bolagets framtid! För rätt person finns stora möjligheter att växa och utvecklas.

Ansökan: Har du rätt kompetens för tjänsten och är nyfiken på att veta mer om Metacon? Skicka in din ansökan genom att klicka på "Ansök nu"-knappen och ta chansen att få träffa oss för att få reda på om Metacon kan vara din nästa arbetsgivare! Har du frågor kring rollen eller företaget är du varmt välkommen att kontakta rekryteringskonsult Martin Winrow, 0760026927. Då urvalsprocessen och intervjuer sker löpande ser vi gärna att du skickar in din ansökan så snart som möjligt.

Varför Metacon? Hos Metacon får du chansen att vara en del av en revolutionerande förändring, bidra till en hållbar planet och arbeta med toppskiktet av experter inom industrin. Med en stark teknologibas är Metacon ledande på den svenska marknaden och siktar på att bli ledande i Europa. Läs mer på Metacon.com.

Ansök nu

Life Science-ingenjör inom processutveckling

Läs mer Apr 22
Företagsbeskrivning
AFRY erbjuder tjänster inom teknik, design, digitalisering och rådgivning. Vi är hängivna experter inom industri, energi- och infrastruktur, som skapar värde för kommande generationer. AFRY har en global räckvidd med djupa rötter i Norden. Tillsammans accelererar vi omställningen till ett mer hållbart samhälle.  


Jobbeskrivning
Hos oss på AFRY tror vi på kraften i olikheter och samarbete. Vi delar idéer och kunskap, utmanar och stöttar varandra att utvecklas vidare. Vi förstår vikten av flexibilitet och en bra balans mellan arbete och fritid.
Är du ingenjör och har erfarenhet av Life Science och att arbeta i industriell- eller labbmiljö och är redo för nästa steg i karriären?
Vi är ett engagerat team som hjälper våra kunder att utveckla framtidens produkter, processer och metoder för Life Science-industrin. Våra uppdrag varierar från utveckling till produktion. Hos oss arbetar vi både tillsammans i större Life Science-projekt och i enskilda konsultuppdrag. Du jobbar framför allt tillsammans med kollegor som har sin expertis inom bioteknik och kemi. Våra kunder uppskattar vår kompetens inom Life Science-industrin och anförtror oss intressanta uppdrag inom processutveckling, uppskalning, test och verifiering
Som konsult hos oss kommer du framför allt fokusera på:
Processutveckling
Uppskalning av processer
Test och verifiering av utrustning och instrument

Sedan kan det såklart utökas med andra intressanta områden. Som Life Science-ingenjör jobbar du brett och fokusområdena kan variera beroende på uppdrag. Vi söker medarbetare till Uppsala, men regelbunden pendling till Stockholm (eller i Mälardalen) kan förekomma.


Kvalifikationer
Vi söker dig som har en teoretisk grund i kombination med ett stort intresse för arbete med kreativ problemlösning. Det kan till exempel handla om att arbeta praktiskt med laborativa uppgifter eller med instrument- och produktionsutrustning.
 Vi ser även att du kan bocka av följande kompetenser/erfarenheter:
Du är utbildad civil- eller högskoleingenjör inom kemi, bioteknik, eller maskinteknik (alternativt motsvarande relevant teknisk-naturvetenskaplig utbildning).
Du har minst 3 års relevant arbetslivserfarenhet inom Life Science-industrin, t ex inom processutveckling, uppskalning av processer, validering av metoder och processer, test och verifiering av utrustning/instrument.
Du har erfarenhet av labb och/eller produktionsmiljö.
Mycket goda kunskaper i svenska och flytande engelska, både i skrift och tal.

Meriterande erfarenheter:
Du har erfarenhet av GMP och/eller ISO. QA/QC, testning och verifiering.
Erfarenhet av reglerad verksamhet och vana av att dokumentera resultat och övrigt arbete enligt rutiner och regelverk.
B-körkort.

För att trivas i rollen behöver du vara driven, självgående och ha lätt för att kommunicera med andra. Du har förmågan att samarbeta och jobba i projektform. Du är strukturerad, analytisk och har förmågan att ta hänsyn till helheten utan att tappa fokus på leveransen. Du uppskattar variation i arbetsuppgifter och att anpassa dig till förändring kommer naturligt.
Sist men inte minst värderar du team work högt, precis som vi!


Ytterligare information
Låter detta som ett spännande nästa steg. Sök redan idag!
Sista ansökningsdag är 2025-05-08. Men tänk på att vi jobbar med löpande rekrytering, vilket innebär att rollen kan tillsättas innan sista ansökningsdag. 
Vi tar inte emot ansökningar via e-mail. Vi undanber oss direktkontakt med bemannings- och rekryteringsföretag samt säljare av ytterligare jobbannonser.
Kontakt vid frågor:
Filip Wirén

Section Manager

filip.wiren@afry.com

På AFRY driver vi förändring i allt vi gör. Vi anser att förändring sker när modiga idéer möts, när vi samarbetar, skapar innovation och omfamnar kreativa lösningar, det är så vi skapar framtiden. Vi söker konstant kvalificerade kandidater som vill ansluta sig till våra inkluderande  team runt om i världen. Bli en del av oss och påskynda den gröna omställningen

Ansök nu

Senior Process Engineer -Aseptic Filling & Visual Inspection

Läs mer Maj 15
Nytt
Do you have deep experience in aseptic manufacturing and visual inspection systems? Are you comfortable stepping in as a subject matter expert when complex technical challenges arise? Galderma is now hiring a Senior Process Engineer with a focus on Aseptic Filling & Visual Inspection to support our continued growth and expansion.



About the role



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

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



Key responsibilities include:

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



What we're looking for



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

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

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



Why Galderma?



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

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

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

Ansök nu

Experienced C&Q Process Engineer

Läs mer Maj 15
Nytt
Looking for real growth in a dynamic, science-driven environment?

We're growing our CQV team at Galderma Uppsala and offer exciting opportunities in validation and engineering.



About Galderma



Galderma is the world's largest independent dermatology company, operating in nearly 90 countries with a portfolio that includes some of the most trusted brands in aesthetics and dermatological care - such as Restylane, Azzalure, and Sculptra.

At our Uppsala site, we offer something unique: the entire value chain - from R&D to manufacturing and global distribution - all in one location. This enables close collaboration, real impact, and rapid innovation.

We are now expanding our CQV (Commissioning, Qualification & Verification) team with an experienced engineer who is ready to grow with us, contribute to quality outcomes, and support our mission to deliver safe and effective dermatological solutions to patients worldwide.



About the Role



As a CQV Engineer, you will be responsible for qualifying and verifying critical manufacturing and utility systems in accordance with GxP standards and internal requirements. You will ensure that systems are designed, installed, tested, and maintained according to regulatory expectations and project timelines.

Key responsibilities include:

* Planning and executing Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for GxP systems.
* Writing, executing, and reviewing qualification protocols and reports.
* Providing support during deviations, change control, and CAPA activities.
* Collaborating closely with production, quality, engineering, and maintenance teams.
* Ensuring all activities follow applicable guidelines such as ASTM E2500, ISPE Commissioning and Qualification Good Practice Guide, and internal SOPs.
* Supporting requalification of systems and continuous improvement of CQV documentation and strategy.



This is a hands-on, on-site role in Uppsala due to the physical access required to systems and equipment.



Required Qualifications and Experience

* 2-5 years of experience in CQV, validation, or engineering within the pharmaceutical or medical device industry.
* Experience with executing and reviewing IQ/OQ/PQ protocols and working under cGMP conditions.
* Familiarity with qualification of cleanrooms, WFI systems, HVAC, gas utilities, cold storage, and aseptic manufacturing equipment.
* Strong knowledge of applicable regulatory frameworks and industry best practices.
* Fluent in both Swedish and English.



Preferred Qualifications

* Experience with computerized system validation (CSV).
* Familiarity with digital validation systems (e.g., ValGenesis, Veeva Vault).
* Experience with serialization, automation systems, or MES platforms such as Pas-X.
* Background in startup or large-scale production environments.
* Enjoyment of structured documentation work and detail-oriented tasks.



What We Offer

* A dynamic, cross-functional working environment with exposure to multiple technologies.
* Access to the full product lifecycle in a single location - from research and development to final manufacturing.
* A collaborative, inclusive culture that values every voice.
* Opportunities for professional growth, internal mobility, and training.
* Competitive salary and comprehensive benefits package.



Why Join Galderma?



At Galderma, you'll have the opportunity to work with world-leading products and technologies in a company that puts science, quality, and patient outcomes first. You'll join a supportive team of professionals who share a common goal - advancing dermatology for every skin story.

Our Uppsala site offers a rare opportunity to be involved in all stages of product development and manufacturing in one of the world's most respected dermatology companies.



Application Process



Apply via our careers page on galderma.com, or, if you're already employed at Galderma, through the internal Workday platform.

Application deadline: April 30, 2025.
We evaluate candidates on an ongoing basis and may fill the role before the deadline.



Ready to be part of something meaningful?
Apply now and help us shape the future of dermatology - one qualified system at a time.

Ansök nu

Senior CSV Engineer

Läs mer Maj 13
CSV Engineer



Do you enjoy making sure systems work as they should and want to contribute to high-quality, compliant solutions?

At Galderma, we're growing our engineering team in Uppsala and are looking for a Computerized System Validation (CSV) Engineer to support both daily operations and long-term projects. With new systems being implemented and existing ones evolving, you'll have the opportunity to join us at a time of exciting development and change, with the opportunity to contribute from the start. Galderma is the world's largest independent dermatology company, offering a science-based portfolio across aesthetics, skincare, and therapeutic solutions in close collaboration with healthcare professionals.



The role

You'll be part of a collaborative engineering team that works closely with colleagues in automation, commissioning, qualification, and quality. The team ensures that hardware installations, software validation, and data management are all compliant, reliable, and well-documented. As a CSV Engineer, your focus will be on the validation and qualification of computerized systems connected to Facility, Utility, and Manufacturing areas. You'll ensure systems are implemented correctly, perform as intended, and meet the relevant regulatory requirements such as GxP and GAMP5.



In this role, you will:

* Function as the SME (subject matter expert) regarding Computerized System Validation and provide guidance to engineers within the organizaition and project teams.
* Plan, write, and execute validation protocols (IQ, OQ, PQ) for computerized systems
* Review system design and functionality to ensure compliance with regulatory requirements and industry standards.
* Perform hands-on testing of systems and interfaces
* Ensure that all OT systems and processes meet, and can be used as intended, according to the required standards and regulations.



Who are you?

To thrive as a CSV Engineer at Galderma, you're someone who values collaboration and enjoys being part of a team working toward shared goals. You bring a positive mindset, are flexible in how you work, and take a structured approach to tasks. You're naturally curious about how systems operate, especially within Operational Technology (OT), and you like making sure they run smoothly, communicate correctly, and meet all the right standards.



We believe you also bring:

* At least 5 years of experience with Computerized System Validation (CSV), ideally from the pharmaceutical or medical device industry, where quality and compliance are part of everyday life.
* Familiarity with GxP environments and frameworks like GAMP5
* Experience creating and executing Plans, Protocols, Test Scripts and Reports as they relate to Qualification and Validation of assigned Computerized systems associated with Facility, Utility and Manufacturing GxP systems throughout their lifecycle.
* Proficency with all the phases of SDLC (System Development Life Cycle), STLC (system testing life cycl) processes, Validation methologies and Concepts of Qualification Documents/ Protocols.
* Fluency in both Swedish and English



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 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 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

Andra jobb i Uppsala från Q-Med AB

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

Production Scheduler

Arbetsledare, tillverkning kemiska produkter
Läs mer Maj 15
Nytt
Production Scheduler
Location: Uppsala, Sweden (on-site)

Job Description
Do you have a strong ability to maintain structure and work with planning in a dynamic environment? Would you like to be part of the planning function within Supply Chain at Galderma? If so, keep reading. We are looking for a Production Scheduler!



Responsibilities:

* Communicate production schedules to relevant departments to ensure all stakeholders are informed and can act accordingly.
* Ensure short- and long-term supply of strategic components and finished products to avoid production interruptions.
* Release and schedule manufacturing orders in the ERP system M3 to effectively implement the production plan.
* Assign new batch numbers to manufacturing orders to ensure traceability and proper handling of products.
* Participate daily in DOR (Daily Operations Review) and batch follow-up meetings to monitor and adjust the production plan as needed.
* Manage deviations within Supply Chain to identify and resolve any issues arising in the production process.
* Drive change requests to ensure continuous improvement and efficiency within production planning.



Qualifications:

* Education in logistics or equivalent work experience.
* Experience in production and/or material planning.
* Proficiency in Swedish and English at a professional level.
* Experience in the pharmaceutical industry is advantageous.
* Good understanding of LEAN principles is a plus.



What We Offer:
You will work for an organization that embraces diversity and inclusion, believing that better outcomes are achieved by reflecting the perspectives of our diverse customer base.

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

At Galderma in Uppsala, we offer you the opportunity to work in an exciting, international environment where both personal and professional development are encouraged. Our offices are situated along the Fyris River in Uppsala, just a 10-minute bike ride from Uppsala Central Station.



Next Steps:
If you are interested, we welcome your application via the "Apply Now" link by June 18, 2025. Selection and interviews are conducted on an ongoing basis during the application period, and the position may be filled before the final application date.

If your profile is a match, we will invite you for an initial conversation with the recruiter.

The next step is an interview with the hiring manager.

The final step is a panel interview with the team.



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

Ansök nu

Process Engineer

Processtekniker, tillverkningsindustri
Läs mer Apr 28
Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.



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

Job Title: Process Engineer
Location: Uppsala, Sweden (onsite)



Job Description

Exciting opportunities await as Galderma seeks a talented Process Engineer to join our innovative team. As a Process Engineer, you will be instrumental in implementing and overseeing engineering plans and programs, contributing to the enhancement of processes across multiple operational areas within Galderma.



Key Responsibilities

*

Implement and manage engineering plans and programs to support organizational activities.
*

Track and ensure alignment of engineering activities with product/process modifications and improvements.
*

Execute engineering processes and policies for the development of new products/processes.
*

Analyze technology trends and contribute to successful deployment of engineering plans, meeting quality, cost, safety, and performance standards.
*

Collaborate on engineering activities to assess feasibility, cost-effectiveness, and customer demand for both new and existing products.
*

Participate in field-testing of products, processes, and systems.



Skills & Qualifications

*

Bachelor's degree in engineering or related field.
*

Hands-on experience on running production in machinery
*

Hands-on on installation
*

Strong experience in engineering operations.
*

Demonstrated ability to work independently with moderate supervision.
*

Strong analytical skills with the ability to solve complex problems through prior experiences.
*

Fluent in Swedish and English



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 450 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

Senior Filling Engineer

Produktionsingenjör, kemi
Läs mer Maj 16
Nytt
Senior Filling Engineer

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



Job Description

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



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



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



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



Ansvarsområden

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



Kvalifikationer:

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



Vi erbjuder

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

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

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



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag, dock senast den 6 juni 2025. Urval och intervjuer görs löpande under ansökningstiden, tjänsten kan komma att tillsättas innan sista ansökningsdatum.

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



Our people make a difference

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

Ansök nu

Automation engineer

Automationsingenjör, maskin
Läs mer Apr 28
At Galderma we're unique and we embrace difference.

Whether it's the unique breadth of our integrated offering that covers Aesthetics, Consumer, and Prescription products; or our commitment to recognising and rewarding people for the contribution they make - working here isn't like anywhere else.



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



Job Title: Automation Engineer

Location: Uppsala, Sweden (on site)



Job description:



As an Automation Engineer, you will manage, plan, and oversee the implementation of engineering plans and programs related to operational automation systems and manufacturing lines, ensuring they meet required safety and performance standards. Your responsibilities will include developing and executing engineering plans, analyzing issues and trends in manufacturing automation systems, and providing reliable solutions to maintain the sustainability of manufacturing lines. Additionally, you will develop and maintain relationships with stakeholders, ensure compliance, support operations, and represent the company in projects and interactions with suppliers. ?



Key responsibilities:

* Provide expert troubleshooting and maintenance support for existing automation systems, ensuring maximum uptime and system performance. Program and configure automation systems, PLCs, HMIs, and SCADA solutions.
* Support Design and develop automation solutions for biopharmaceutical manufacturing processes.
* Collaborate with cross functional teams to ensure alignment with site and project requirements.
* Implement best practices for system reliability, scalability, and (OEE) Overall Equipment efficiency.
* Create automation related change controls and execute CSV activities.
* Investigate automation related deviations and support other deviations.
* Identify opportunities for process optimization and continuous improvement.
* Perform automation computer system support activities (e.g., system backups, performance monitoring, password maintenance, etc.)
* Provide technical support for automation control system platforms and/or process information systems (e.g., data historians).
* Execute all work in a manner consistent with GMP and Galderma policies, procedures, and standards.
* Technical and firsthand automated equipment troubleshooting, repair, and improvements. Lead in root cause and corrective action (RCCA).
* Good knowledge of project management process.
* Conform with and abides by all regulations, policies, work procedures, instruction, and all safety rules. Assist in regulatory and internal Compliance audits.



Skills & Qualifications

* Bachelor's degree in electrical, control or electronic engineering
* Minimum of 3 years' experience in automation configuring automation systems, PLCs, HMIs, and SCADA solutions.
* Previous experience within GMP and Part 11 or alternatively from a related regulatory industry.
* Experience with SCADA systems, historian, Siemens, WinCC, iFix, Wonderware, etc.
* Experience in capital project execution and machinery/system design.
* Professional level in English, desirable 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

Senior Sterilization Engineer

Produktionsingenjör, kemi
Läs mer Maj 16
Nytt
Senior Sterilization Engineer

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



Job Description

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



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



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



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



Ansvarsområden

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



Kvalifikationer:

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



Vi erbjuder

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

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

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



Nästa steg
Har vi fångat ditt intresse? Vi välkomnar din ansökan via länken "Apply Now / Ansök nu" redan i dag, dock senast den 6 juni 2025. Urval och intervjuer görs löpande under ansökningstiden, tjänsten kan komma att tillsättas innan sista ansökningsdatum.

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



Our people make a difference

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

Ansök nu

Process Engineer (Aseptics)

Civilingenjör, process, kemiteknik
Läs mer Apr 28
Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.



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



Job Title: Process Engineer (Aseptics)
Location: Uppsala, Sweden (onsite)



Job Description

Join Galderma as a Process Engineer, where you'll play a key role in enhancing our operations. With a focus on aseptic processes, you will apply your expertise to optimize production systems, uphold safety and compliance, and collaborate with cross-functional teams.



Key Responsibilities

*

Develop, implement, and optimize aseptic manufacturing processes to meet quality, safety, and compliance standards.
*

Collaborate with cross-functional teams to analyse and resolve technical challenges in production, leveraging prior experience and innovative thinking.
*

Support engineering activities to modify and improve existing aseptic processes, develop new test procedures and policies for aseptic environment, ensuring alignment with operational goals
*

Participate in risk analysis and troubleshooting, maintaining focus on aseptic standards to ensure contamination-free operations.
*

Monitor technology trends and support the deployment of engineering solutions that enhance reliability, cost-effectiveness, and efficiency.
*

Provide technical support during audits and inspections, ensuring adherence to regulatory and company standards.



Skills & Qualifications

*

Bachelor's Degree in Engineering with work experience within pharma, or Bachelor's Degree in Biology, Chemistry with experience from working with process engineering, or equivalent experience.
*

Some years of experience from industry, preferably within aseptic manufacturing.
*

Strong problem-solving skills and the ability to work independently with moderate supervision.
*

Familiarity with quality standards and risk management processes in regulated environments.
*

Fluent in Swedish and English.



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. If you are currently an employee of Galderma, we welcome your application via our internal career site via Workday. The selection process is ongoing and the role may be filled prior the last application date.



*

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

The next step is a virtual conversation 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