Regulatory Affairs jobs in the Netherlands
Regulatory Affairs jobs involve ensuring that an organization complies with the regulations and guidelines set forth by regulatory authorities in their respective industry. This can include pharmaceuticals, medical devices, biotechnology, cosmetics, food, or any other industry that is subject to government regulations. Regulatory Affairs professionals work to ensure that products meet regulatory requirements for safety, efficacy, and quality. They research and interpret regulations, provide guidance to internal teams on compliance matters, and develop strategies to navigate the regulatory landscape. They also prepare and submit regulatory filings, such as applications, reports, and dossiers, to gain necessary approvals, licenses, and permits. Regulatory Affairs professionals monitor and stay up to date with changes in regulations, assess the impact of regulatory changes on products and the company, and implement necessary adjustments to maintain compliance. They may also liaise with regulatory authorities, participate in regulatory inspections or audits, and respond to queries or requests for information. Strong attention to detail, knowledge of regulatory guidelines and requirements, and excellent communication and project management skills are essential for success in Regulatory Affairs jobs. These professionals play a critical role in ensuring the safety and quality of products, maintaining compliance with regulations, and facilitating the timely market access of products.
Found jobs - 36
Exact matches
- Senior Director, Regulatory Affairs Strategy-EU/RoWGenmab - Utrecht, Netherlands; Copenhagen, DenmarkPosted 30+ days ago
- Associate Director Regulatory Affairs CMC (36-40 hrs)Merus - Utrecht, NetherlandsPosted 30+ days ago
- Associate Director/Director - Regulatory Affairs (EMA expert)Medpace - NetherlandsPosted 30+ days ago
- Associate Director/Director - Regulatory Affairs (EMA expert)Medpace - Rotterdam, Netherlands; Leuven, BelgiumPosted 30+ days ago
- (Senior) Regulatory Affairs OfficerBilthoven Biologicals - Bilthoven, NetherlandsPosted 30+ days ago
Related matches
- Principal Prof, Clinical Quality Management Specialist - Fully remote / urgent needSyneos - Netherlands5 days old
- Manager Level - Quality Operations Lead (80-100%)Johnson & Johnson - Nijmegen, Netherlands28 days old
- Deputy European Union (EU) Qualified Person for Pharmacovigilance (m/f/d)Lilly - 14 Locations29 days old
- Senior Specialist Global Trade ComplianceOrganon - Amsterdam, Netherlands; Brussels, BelgiumPosted 30+ days ago
- QC Technician / Laboratorium medewerkerThermo Fisher Scientific - Tilburg, NetherlandsPosted 30+ days ago
- Senior Manager, BiostatisticsGenmab - Utrecht, Netherlands; Copenhagen, Denmark; Princeton, United StatesPosted 30+ days ago
- System Compliance Manager, Digital Systems Management, Veeva VaultsGenmab - Utrecht, Netherlands; Copenhagen, Denmark; Princeton, United StatesPosted 30+ days ago
- System Manager, Digital Systems Management, Veeva QualityGenmab - Utrecht, Netherlands; Copenhagen, Denmark; Princeton, United StatesPosted 30+ days ago
- Product Stewardship, Senior SpecialistThermo Fisher Scientific - Bleiswijk, Netherlands; Loughborough, United KingdomPosted 30+ days ago
- Associate Director, RA Labeling Product Leader (1 of 2)Johnson & Johnson - 10 LocationsPosted 30+ days ago