Vacatures regulatory affairs in Almere

We anticipate the application window for this opening will close on - 30 Oct 2026 At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down barriers to innovation for a more connected, compassionate...

pAs a Regulatory Affairs Specialist at Sandoz, you will work on registrations, product information and artworks for existing and future products. You combine attention to detail with strong planning skills and collaborate with a range of internal and external stakeholders. /p h3What will you do? /h3 pAs a Regulatory Affairs Specialist, you ensure that our...

pJob Description Summary At Sandoz, our Purpose is pioneering access for patients /ppJob Description As a Regulatory Affairs Specialist at Sandoz, you will work on registrations, product information and artworks for existing and future products. You combine attention to detail with strong planning skills and collaborate with a range of internal and external...

pSandoz B.V. is seeking a Regulatory Affairs Specialist to manage registrations, product information, and artworks for current and future products. /ppYou will combine meticulous attention to detail with strong planning and collaborate with a wide range of internal and external stakeholders. You will ensure compliance with registration requirements,...

pSandoz is seeking a Regulatory Affairs Specialist in the Netherlands, based in Almere. You will ensure product registrations, official product information, and artwork alignment across the product portfolio, working with internal and external stakeholders to deliver compliant documentation. /ppYou bring a degree in biomedical sciences or pharmacy,...

Job Description SummaryThis job advert is in two languages: English and DutchJob DescriptionVacaturetekst in het NederlandsWil jij bijdragen aan de registratie en beschikbaarheid van geneesmiddelen en jezelf verder ontwikkelen binnen Regulatory Affairs? Als Country Regulatory Affairs Specialist bij Sandoz werk je aan registraties, productinformatie en...

pAt UL Solutions, we're helping organizations navigate one of the most significant sustainability and compliance transformations in Europe. /p pUL Solutions is seeking a highly motivated and experienced Program Owner, EU Battery Regulation Digital Product Passport (DPP) to lead the development, implementation, and growth of our Battery Regulation conformity...

As a Regulatory Affairs Specialist at Sandoz, you will work on registrations, product information and artworks for existing and future products. You combine attention to detail with strong planning skills and collaborate with a range of internal and external stakeholders. What will you do? As a Regulatory Affairs Specialist, you ensure that our products...

pAs a Regulatory Affairs Specialist at Sandoz, you will work on registrations, product information and artworks for existing and future products. You combine attention to detail with strong planning skills and collaborate with a range of internal and external stakeholders. /h3 pAs a Regulatory Affairs Specialist, you ensure that our products and the related...

Sinclair is Hiring! Join Our Team as Chief Development Officer.Location: Flexible across Europe (Preferred: Netherlands, UK, Germany, Italy, Spain or France)Role PurposeThe Chief Development Officer (CDO) is a member of the Executive Leadership Team and is responsible for leading the Company's global Quality, Regulatory Affairs, Vigilance and Product...

Job Description SummaryJoin us, the future is ours to shape!Job DescriptionThe Operations Publishing team is responsible for the delivery of published output which fulfils the technical and format requirements of the Health Authorities and is dispatched and / or submitted to the authorities according to given timelines and in high quality. of regulatory...

ppbWorking hours: /b 40 (possible to work from home 2 days), PV 20 hours RA 20 hours /p pbDepartment: /b Medical /p pbReports to: /b Quality and Regulatory Affairs Manager /p h3Position Summary /h3 pAs Pharmacovigilance Regulatory Affairs Officer you will supports the daily activities of Pharmacovigilance (PV) and Regulatory Affairs (RA) within a regulated...

A pharmaceutical company in Almere, Netherlands is seeking a Pharmacovigilance Regulatory Affairs Officer to support key safety and registration processes within a regulated environment. The ideal candidate must be fluent in Dutch and English and have 1-3 years of experience in pharmacovigilance or regulatory affairs. Responsibilities include recording...

ph3Job Description Summary /h3pJoin us, the future is ours to shape! /ph3Job Description /h3pYour Key Responsibilities: /pulliDeveloping evidence-based policy positions for regulatory requirements for ethical and efficient development and manufacturing of generic and biosimilar medicines. /liliAligning Sandoz policy objectives and advocacy plans within...

pSandoz B.V in the Netherlands seeks an experienced Regulatory Affairs professional to shape policy for generic and biosimilar medicines. You will lead regulatory strategy, interact with Health Authorities, and coordinate industry collaboration. /ppThe role covers developing evidence-based policy positions, advising development teams, and representing Sandoz...

Company Description Guardant Health is a leading precision oncology company focused on guarding wellness and giving every person more time free from cancer. Founded in 2012, Guardant® is transforming patient care and accelerating new cancer therapies by providing critical insights into what drives disease through its advanced blood and tissue tests,...