Uppsala: Senior Sterilization Engineer

Some of the things you’ll do
We are looking for production technicians to join us in the scale up of our sodium-ion battery cell manufacturing facility! The Production Technician is responsible for operating, maintaining, and troubleshooting equipment on the battery cell assembly line. This role ensures the efficient and accurate production of battery cells while adhering to safety and quality standards. The Production Technician will work closely with engineers and other team members to optimize production processes, conduct quality checks, and contribute to continuous improvement initiatives.
Key responsibilities inclute but are not limited to
Operate manufacturing equipment and machinery to produce battery cells according to production schedules and specifications.
Follow detailed work instructions and standard operating procedures (SOPs) to ensure consistent and accurate assembly of battery cells.
Conduct regular inspections and quality checks on battery cells and components to ensure they meet required standards and specifications.
Identify and troubleshoot equipment malfunctions and process deviations, working closely with engineers and other team members to resolve issues promptly.
Maintain accurate records of production activities, including work performed, materials used, and any issues encountered.
Adhere to all safety protocols and guidelines, including the proper handling of chemicals and materials, and ensure the regular cleaning and maintenance of machines, to maintain a safe and efficient work environment.
Participate in continuous improvement initiatives, providing feedback on production processes and suggesting enhancements to improve efficiency, quality, and safety.
Willingness to work in different areas of production as needed, demonstrating versatility and adaptability to changing production requirements.


What Were looking for
A high school diploma or equivalent is required.
Experience working in a manufacturing environment.
Basic knowledge of electrical and mechanical systems.
Vocational or technical training related to manufacturing, electronics, or a related field is highly beneficial.
Good written and verbal communication skills (English).
Proficiency in operating and troubleshooting manufacturing equipment.
Ability to read and interpret technical manuals, schematics, and work instructions.
Competence in using basic hand tools and measurement instruments.
Basic computer skills, including proficiency in Microsoft Office software (Excel, Word, etc.) for data entry, report generation, and documentation.
Knowledge of industry safety protocols and the ability to maintain a safe working environment.
Ability to work independently and collaboratively in a team environment, with effective communication skills.
This position requires on-site presence Monday to Friday, 8:00 AM – 5:00 PM.

What you will get
We can promise you that you will be challenged, develop your skills and have the opportunity to work with truly amazing and competent colleagues. If you like changes and want to set new processes and ways of working - this is the place for you!
Diversity and inclusion are very important to us and we are committed to creating an inclusive work environment. We want to be a workplace where everyone’s perspectives and opinions are valued, and we are dedicated to creating opportunities for all employees to thrive and reach their full potential.

QRIOS söker en Produktionsingenjör för ett spännande konsultuppdrag hos vår kund Cytiva i Uppsala och till deras kemiska produktion. Låter det intressant? Tveka inte ansöka då urval samt intervjuer sker löpande.

Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Deras kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.

Om tjänsten
Vi söker en Produktionsingenjör till sektionen Renrumsproduktion - en del av den kemiska produktionen på Cytivas fabrik i Uppsala. Gruppen som vi söker Produktionsingenjör till arbetar med att tillverka “Ready to Process” kromatografikolonner. Produktionen sker i ISO-klassat renrum.

Att arbeta som Produktionsingenjör hos Cytiva betyder framför allt att du är ett dagligt stöd till produktionen. Rent praktiskt kan det innebära att du arbetar med att:
• Daglig uppföljning av produktionen.
• Driva Change Control-ärenden och avvikelsehantering.
• Teknisk felsökning av processutrustning.
• Kontakt med underhållsavdelning och/eller entreprenörer.
• Samarbeta med F&U vid nyproduktprojekt och produktvårdsprojekt.
• Agera som stöd i reklamationsärenden och driva utredningar rörade reklamationer.

Du driver även förbättringsarbete, uppdaterar produktionsdokument samt utför och dokumenterar riskanalyser mm. Ingenjörsarbetet präglas av variation och en möjlighet till att påverka den dagliga verksamheten, där tillverkningen står i fokus.

Dina arbetsuppgifter i huvudsak
De huvudsakliga kraven för tjänsten är:
• högskoleingenjör eller motsvarande med inriktning mot bioteknik/kemiteknik/maskinteknik eller liknande utbildningsbakgrund, alternativt relevant erfarenhet som kan motsvara universitetsutbildning.
• Du behärskar svenska och engelska flytande i tal och skrift.
• God datorvana och trygg användare av olika IT-system.

Det är även meriterande om du har tidigare erfarenhet av:
• GxP kunskap
• Erfarenhet av kolonnpackning
• Erfarenhet av processindustri/läkemedelsindustri

För att vara framgångsrik i denna roll ser vi gärna att du är en lagspelare med god samarbetsförmåga och att du trivs i med att jobba både med teknik och med människor. Vidare ser vi gärna att du är en säkerhets- och kvalitetsmedveten person med god förmåga att ta initiativ och driva flera parallella aktiviteter samtidigt

QC Specialist

Location: Uppsala, Sweden on-site.



Job Description

Bli en del av Galdermas framgångsrika tillväxtresa - utvecklas i rollen som QC Specialist!



Vi söker en engagerad och lösningsorienterad QC Specialist till kvalitetskontrollavdelningen på Galderma i Uppsala. Som QC Specialist får du ett övergripande ansvar för att säkerställa att vår verksamhet uppfyller högt ställda kvalitets- och GMP-krav. Du kommer att driva arbetet med avvikelser, CAPA och CC-ärenden, samtidigt som du är en viktig kontaktperson i projektförfrågningar och samverkan med andra avdelningar i QC-relaterade frågor. Du kommer att höra till gruppen QC Chemistry Finished Products men ha ett nära samarbete med QC Specialister i övriga QC grupper.



Rollen innebär att du är ett specialiststöd för gruppen och snabbt tar dig an uppgifter som kräver både bredd och djup kompetens. Att ta fram riskanalyser, utredningar och andra underlag av hög kvailtet är en viktig del i ditt arbetet. Du ansvarar även för QC-acceptans av våra analyssvar samt bidrar till att driva förbättringsarbete inom kvalitetsprocesserna. Det här är en roll för dig som trivs med att kombinera operativt arbete med rådgivning och som vill vara en nyckelperson i ett starkt och kunnigt team.



Teamet består i dag av 17 personer med kompetens inom kvalitetskontroll med inriktning mot kemiska analyser av slutprodukt. Gruppen inkluderar en QC-specialist, två QC-specialister med fokus på metoder samt ett flertal QC-analytiker som arbetar laborativt. Tillsammans utgör de en viktig del av Galdermas kvalitetskontroll.



Ansvarsområden

* Rapportera, utreda och dokumentera avvikelser, genomföra korrigerande och förebyggande åtgärder
* Driva och dokumentera ändringsärenden
* Utföra QC acceptans och statussättning
* Samordna projektinsatser för gruppen
* Representera verksamheten vid inspektioner och annat regulatoriskt arbete
* Följa upp och analysera kvalitetsrisker och leveransförmåga samt säkerställa att åtgärder identiferas och genomförs vid behov
* Vara aktiv och drivande i förändrings- och förbättringsarbete med målsättning att skapa en effektiv kvalitetskontroll med hög leveransförmåga



Kvalifikationer:

* En naturvetenskaplig bakgrund, gärna inom kemi
* Erfarenhet av att arbeta inom GMP-reglerad verksamhet, exempelvis inom läkemedels- eller medicinteknisk industri
* Laborativ erfarenhet, gärna från kvalitetskontroll eller annat reglerat analysarbete
* God förmåga att hantera, utreda och driva avvikelser
* God kommunikationsförmåga, både i tal och skrift
* Goda kunskaper i svenska och engelska, både i tal och skrift



Vi söker dig som har mod att utmana kända processer, som tar initiativ till förbättringar och som vill bidra till en mer effektiv kvalitetskontroll. Du är lätt att samarbeta med, har en stark teamkänsla och kundfokus samt ha ett noggrant och kvalitetsmedvetet arbetssätt. Vi sätter stor viktigt vid dina personliga egenskaper samt förmåga att planera och prioritera ditt arbete på ett effektivt sätt.



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 14 juli 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.
* Därefter följer en intervju med anställande chef
* Nästa steg kan vara en intervju med några ur teamet och/eller en annan QC-chef
* Slutligen genomför vi 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.

Job Title: Technology Transfer Lead
Location: Uppsala, Sweden (on site)

Job description:
The Technology Transfer Lead will provide oversight on all aspects of technology transfer (TT) programs with key stakeholders to ensure the smooth and efficient transfer of new products, processes, or technologies from R&D to production and other operational units. He will manage and facilitate the transfer of knowledge, technologies, and processes from development to production or from one department or facility to another.



Key responsibilities:

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Site representation in global technology transfer process
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Implement programs for smooth transition of products from R&D into full production readiness, representing MS&T in Tech Transfer projects.
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Subject matter expert (SME) for Technology Transfer and Process Validation strategies.
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Collaborate with the team to ensure that proposed transfer optimizes the production process in terms of process efficiency, cycle time, reliability, and serviceability.
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Technology Transfer Management: Lead and coordinate the end-to-end process of transferring technologies from R&D to production or across sites. Develop transfer strategy and implement technology transfer plans, including timelines, key milestones, and risk assessments. Collaborate with process development, engineering, and quality teams to ensure the scalability and robustness of new technologies. Ensures all deliverables are in place prior to each project milestone.
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Project Management: Create detailed project plans and timelines for tech transfer activities and communicate progress to stakeholders. Track project deliverables, identify and address roadblocks, and ensure all actions are completed on time.
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Documentation & Compliance: Ensure all technology transfer documentation, including standard operating procedures (SOPs), batch records, and validation protocols, are completed and approved. Ensure compliance with regulatory standards (e.g., FDA, EMA) for the transfer of new technologies. Work with the quality assurance and all support groups to oversee the validation and qualification of new equipment and processes.
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Cross-Functional Collaboration: Coordinating subject matter experts within Development, MS&T, Engineering, and other site related functions or experts and collaborate with cross-functional teams, including quality assurance, regulatory affairs, and process development, to ensure that new technologies meet all quality, regulatory, and operational requirements. Provide technical oversight and support.
*

Troubleshooting & Problem Solving: Identify potential risks in the technology transfer process and develop mitigation strategies. Provide technical support during process scale-up and commercialization phases, troubleshooting issues as they arise.
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Training & Support: Ensure that operational teams are adequately trained on new processes, technologies, or equipment. Provide technical expertise and leadership to teams throughout the transfer and scale-up phases.
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Continuous Improvement: Lead efforts to continuously improve technology transfer processes, ensuring the implementation of best practices. Evaluate and implement process improvements to reduce transfer time and enhance product quality.



Skills & Qualifications

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PhD/ Master / bachelor's degree in in a relevant scientific or engineering field, such as Chemistry, Biochemistry, Chemical Engineering
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Minimum of 6 years of experience in a pharmaceutical, biopharmaceutical, or manufacturing environment, with knowledge of regulatory standards and GMP guidelines.
*

Very good knowledge of drug substance and/or drug product manufacturing.
*

Previous work in compounding, filtration, sterilization, filling and packaging.
*

Experience including process validation, transfer, commercialization and manufacturing support and troubleshooting.
*

Experience with root cause analysis (RCA), risk management tools, quality systems (deviations, CAPA, etc.)

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 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.

Location: Uppsala, Sweden

Are you ready to take your project management career to the next level? Join Galderma, a global leader in dermatology and aesthetic treatments, and lead capital investment projects that make a real impact in the medical device and pharmaceutical industries.



Role Overview:

As a Senior Project Manager, you will manage various types of investment programs and projects to support the commercial production of medical devices and pharmaceutical products. You will lead, plan, organize and coordinate programs and projects activities to deliver according to scope, time line and budget from start to finish in accordance with company practices. This role offers an exciting opportunity to be part of a dynamic team that works across different angles of investment projects, from conceptual design to execution and beyond.



Key Responsibilities:

* Manage capital investment projects with full budget and timeline responsibility.
* Implement processes to ensure successful program and project delivery, meeting scope, quality, and budget constraints.
* Collaborate with cross-functional teams to execute best practices and policies.
* Lead and support teams (3-100 people) ensuring adherence to project methodologies and standards.
* Monitor project status and provide consolidated financial and performance reports to stakeholders.
* Influence key stakeholders and build strong, trusting relationships across departments.
* Drive continuous improvement through process design and solutions for complex challenges.



Key Competencies & Skills:

Required:

* Strong experience (8+ years) in managing capital investment projects, including process equipment, filling lines, packaging lines, and clean room construction.
* Proficient in project lifecycle management, including Conceptual Design, Basis of Design, Detail Design, Execution, Testing, and Start-Up.
* Excellent communication and leadership skills with a team-oriented mindset.
* Extensive experience in Biotech, Pharmaceutical, and Medical Device manufacturing.
* Proficiency in English and Swedish.

Nice to have:

* Technically curious and eager to learn about new technologies and processes.



Why Join Galderma?

At Galderma, you'll work in a supportive, growth-oriented environment with opportunities for professional development. You'll be part of a company committed to diversity and inclusion, where we embrace different perspectives to deliver better outcomes. Galderma's Uppsala site offers a unique edge with the entire product chain from research and development to production and marketing. Work with world-leading brands like Restylane, Azzalure, and Sculptra!



What We Offer:

* Competitive salary and benefits.
* Leadership development programs and career advancement opportunities.
* A collaborative and inclusive work culture.
* A chance to contribute to the global success of Galderma.



Next steps

We welcome your application via our company website. If you are currently an employee of Galderma, we welcome your application via our internal career site via Workday. Apply as soon as possible though no later than the 30th of April 2025. 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