Regulatory System Manager hos Cytiva i Uppsala
Tolkar regelverk för produkter, processer och procedurer samt tar fram strategier för regelefterlevnad. Du har en kandidatexamen i kemi, biokemi eller motsvarande samt erfarenhet av produktregleringar eller QA/RA.
Titel, arbetsplatsens namn och sammanfattning skrivna av AI utifrån annonsen.
Bra att veta
Lön
Inom yrkesgruppen Farmakologer och biomedicinare har de som jobbar i privat sektor i Östra Mellansverige i snitt 60 200 kr i månaden, varav 60 000 kr i grundlön. I hela landet, i privat sektor, tjänar hälften mellan 54 300 kr och 82 200 kr. Det är statistik för yrket, inte vad den här arbetsgivaren betalar.
Källa: SCB, lönestrukturstatistik 2025
Anställningen
Anställningen har inget slutdatum. Den kan börja med en provanställning på högst sex månader. Vill arbetsgivaren avsluta den under provtiden ska du få besked minst två veckor i förväg; annars blir den en vanlig tillsvidareanställning när provtiden är slut. Därefter krävs sakliga skäl för att säga upp dig, och uppsägningstiden är minst en månad, längre ju längre du har varit anställd.
Ett kollektivavtal kan ge andra regler än lagen.
Texten är skriven med AI och kan innehålla fel. Kontrollera med arbetsgivaren.
Källa: Lagen om anställningsskydd (LAS)
Arbetsgivaren
Cytiva har annonserat 54 jobb det senaste året: 52 tillsvidareanställningar, 1 tidsbegränsad anställning och 1 vikariat. Inom yrkesgruppen Farmakologer och biomedicinare har de annonserat 8 gånger de senaste två åren, den här annonsen inräknad.
Källa: vår sammanställning av Arbetsförmedlingens annonser
Regulatory System Manager
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
As a Regulatory System Manager you'll get the chance to interpret different regulations as they apply to Cytivas products, processes and procedures. You will also advise on impact of regulations, devises strategies for compliance, and liaison with regulatory bodies. The position will also work with investigations and resolve compliance problems, questions and complaints. Audits and evaluates current policies, procedures, and documentation will also be a part of the responsibilities.
This position reports to the Sr. Regulatory Manager for chemical and consumable products and is a part of the Product Regulatory Compliance department located in Uppsala.
What You'll Do
Maintain and manage regulatory documentation used in NPDs (New Product Development) to secure compliance to relevant regulations for market access, e.g. safety data sheets
Coordinate and collaborate with IT to ensure regulatory systems are up to date and integrated with other Cytiva systems, including acquired businesses
Support other users of regulatory systems in how to best create compliant documentation
Monitor and review change requests/orders and regulatory changes to ensure that compliance requirements are met and maintained.
Drive simple, cost-efficient and pragmatic solutions to issues related to regulatory requirements in NPDs and other projects.
Who you are
- Bachelors' Degree in Chemistry, Biochemistry or related field with a few years relevant working experience
Experience with Product regulations, QA/RA, other regulatory areas or experience with Cytiva's product portfolio and an interest to learn about regulatory compliance.
Knowledge around the Cytiva portfolio
- Knowledge around environmental and chemistry regulations, e.g. familiar with REACH, GHS labeling, hazardous chemicals, and similar regulations
- Familiarity and interest in maintaining IT systems
It would be a plus if you also possess previous experience in:
- Communicating with authorities, e.g. chemistry and border control authorities
- Written and spoken Swedish
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