Regulatory Affairs jobs
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 - 1511
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Senior Regulatory Affairs Administrator - Central Regulatory Affairs (CRA)Viatris - Lisbon, Portugal2 days old
Regulatory Affairs Manager - Central Regulatory Affairs (CRA), EuropeViatris - Lisbon, Portugal2 days old
Regulatory Affairs Executive - Central Regulatory Affairs (CRA), EuropeViatris - Lisbon, Portugal2 days old
Regulatory Affairs Executive - Central Regulatory Affairs (CRA), EuropeViatris - Lisbon, Portugal2 days old
Associate Regulatory Affairs Executive - Central Regulatory Affairs (CRA), EuropeViatris - Lisbon, Portugal2 days old
Principal Regulatory Affairs Specialist (Global Clinical Trial Applications)Thermo Fisher Scientific - Kyiv, Ukraine2 days old
Senor Scientist, Product Lead CMC Regulatory AffairsJohnson & Johnson - Warsaw, Poland; Beerse, Belgium2 days old
Regulatory Affairs Manager/Senior Manager – CMC & Regulatory Change Management - FSPThermo Fisher Scientific - Milan, Italy2 days old
Regulatory & Submissions Lead (Clinical Operations Manger) - Paris, France (Hybrid) - FSPParexel - France7 days old
Sponsor Dedicated Regulatory Portfolio Snr. Regulatory Consultant (GRO RPSM) open to Spain, Portugal and UK locationSyneos - Madrid, Spain7 days old
Sponsor Dedicated Regulatory Portfolio Snr. Regulatory Consultant (GRO RPSM) open to Spain, Portugal and UK locationSyneos - Barcelona, Spain7 days old
Sponsor Dedicated Regulatory Portfolio Snr. Regulatory Consultant (GRO RPSM) open to Spain, Portugal and UK locationSyneos - United Kingdom7 days old
Senior Manager, Global Regulatory Operations, Process & ComplianceGenmab - Copenhagen, Denmark8 days old
(Senior) Medical Writer in Scientific Publications, Regulatory, Quality & Clinical Reporting, SøborgNovo Nordisk - Søborg, Denmark8 days old
Senior Specialist Regulatory Operations (Electronic Submissions)Viatris - Lisbon, Portugal9 days old
Principal Scientist, CMC Regulatory Affairs - Combination Products (1 of 2)Johnson & Johnson - Allschwil, Switzerland13 days old
Regulatory Principal Specialist, RA CMC Development, CopenhagenNovo Nordisk - Søborg, Denmark14 days old
Associate Director, Regulatory Affairs - Digital Health, Device & Combination Products (all gender)Merck - Eysins, Switzerland20 days old
Regulatory Affairs Specialist/Regulatory Scientist - FSPThermo Fisher Scientific - Belgium21 days old















