Regulatory Strategies Jobs in UK

Job DescriptionRegulatory Affairs SpecialistLocation: Hybrid Kent/LondonJob Type: Full-time PermanentAbout the RoleAn exciting opportunity has arisen for a Regulatory Affairs Specialist to join a growing and collaborative quality team within an international ingredients and nutrition solutions busi...

Job Title: Director Process Engineering & PackagingLocation: Cambridge Biomedical Campus UKHybrid Working model - 3 days per weekIntroductionJoin AstraZeneca Biologics as a Process Engineering & Packaging Leader and drive innovation in biopharmaceutical process development and technology transfer ac...

Job Title: Director Process Engineering & PackagingLocation: Cambridge Biomedical Campus UKHybrid Working model - 3 days per weekIntroductionJoin AstraZeneca Biologics as a Process Engineering & Packaging Leader and drive innovation in biopharmaceutical process development and technology transfer ac...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Molecule Steward (Senior Director) Long-Acting InjectablesBusiness IntroductionWe manufacture and supply reliable high-quality medicines and vaccines to meet patients needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicine...

Title:Senior Medical WriterCompany:Ipsen Biopharm LtdAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience with global hubs...

About This Role:As the Senior Manager Global Regulatory Affairs you will join a dynamic team dedicated to navigating regulatory pathways at an above-market level. You will oversee the preparation submission and management of key regulatory submissions together with the EU Regulatory Lead ensuring co...

The job holder is responsible for managing end-to-end preparation of regulatory registration requirements needed for Health authority submissions across multiple markets ensuring timely highquality deliverables that meet regulatory authority expectations applicable guidance and GSK processes includi...

The job holder is responsible for managing end-to-end preparation of regulatory registration requirements needed for Health authority submissions across multiple markets ensuring timely highquality deliverables that meet regulatory authority expectations applicable guidance and GSK processes includi...