Vacatures regulatory in Almere

h3Job Description Summary /h3 pAt Sandoz, our Purpose is pioneering access for patients /p h3Job Description /h3 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...

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...

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...

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...

Heb jij een achtergrond in het financieel toezichtrecht en wil je de volgende stap zetten in een toonaangevende Band 1-praktijk? Kom dan werken in een team waar inhoudelijke kwaliteit en een prettige, collegiale werksfeer samengaan. Sluit je aan bij het Financial Regulatory team van Houthoff. Wat ga je doen als advocaat-medewerker Financial Regulatory? Als...

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...

Overview In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international...

pSandoz is seeking a Regulatory Affairs Specialist in the Netherlands to manage registrations, product information and artworks for existing and future products. You will combine meticulous attention to detail with strong planning skills while collaborating with internal and external stakeholders. /ppIn this highly regulated environment you will maintain...

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,...

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...

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...

MCO Health BV (part of the Nestlé Group) is a leading player in the field of nutritional supplements and is active in the Netherlands with advisory brands such as Orthica and AOV. MCO is part of Swiss Nestlé Health Science. MCO’s mission is to safeguard optimal human health. Our commitment to good health means more than just offering some of the most...

Seeking a Regulatory Compliance Specialist to manage regulatory documents and product registrations for export markets. Requires a degree in Food Science or Pharmacy and 3-5 years of experience.

Overview In this role you enable medicinal innovations by conducting rigorous on-site monitoring and site management for clinical studies. You'll work within our Functional Services Provider team to ensure protocols and regulatory requirements are met, while collaborating with cross-functional partners. The position focuses on data integrity, regulatory...

Overview In this role you will lead enterprise quality controls and process improvements to elevate supplier quality and ensure regulatory compliance. You will coordinate cross-functionally with R&D, manufacturing, and regulatory affairs to close process gaps and maintain high quality standards. You will oversee NPI validations, process development, and...

Overview In this role you lead a multi-country Regional Research team to shape the region's research, innovation, and academic collaboration agenda, driving scientific advancement and business growth. You will build and manage strategic partnerships with academia, healthcare providers, and government bodies, while engaging executive stakeholders to...

Overview In this role you lead design quality activities for AI-enabled software products across the full lifecycle. You partner with multidisciplinary teams to embed quality and regulatory compliance, ensuring safety, performance, and reliability. You shape quality strategies, KPIs, and robust verification for software and AI models, including data...

Overview As a Clinical Research Associate II at Precision for Medicine, you will oversee site performance to ensure studies are conducted per protocol and regulatory standards. You'll work remotely in the Netherlands with site visits to monitor progress and support study setup. You'll collaborate with cross-functional teams to mitigate risks and maintain...

Overview In this role, you will lead QA/QC for a major hyperscale data centre project in Amsterdam, ensuring compliance with regulatory, client, and project specs. You will oversee inspections, testing, and handover deliverables, and coordinate commissioning with internal and external stakeholders. The position requires strong technical expertise,...