Regulatory Documents Jobs in UK
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Regulatory Labelling Specialist
Idibu
Talentmark are recruiting for a Regulatory Labelling Specialist to join a leading pharmaceutical company on a 12-month contract. Salary:21.10 per hour PAYE or 27.63 per hour Umbrella. Regulatory Labelling Specialist Role:Prepare and update labelling documents for assigned markets.Produce regulatory...
Sr Clinical Scientist
Galderma
Galderma is the emerging pure-play dermatology category leader present in approximately 90 countries. We deliver an innovative science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics Dermatologic...
Bioanalytical Program Lead (principal Scientist) C...
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionBioanalytical Program Lead client dedicatedLocation: UK or Sweden (remote/home based)Thermo Fishers clinical research business is a leading global contract research organization and world leader in serving science. We are p...
Senior Regulatory Affairs Specialist
Coopercompanies
DescriptionJob title: Senior Regulatory Affairs SpecialistDepartment: Regulatory AffairsLocation: Southampton UK or Gothenburg SwedenGLS: P03Working hours: 37.5 hours (UK) or 40 hours (Europe) per week Monday to FridayA brighter future awaits youJob SummaryThe Senior Regulatory Affairs Specialist wi...
Clinical Trial Coordinator
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and...
Enterprise And Liquidity Risk Managing Director
Mizuho
Profile SummaryA senior risk professional with extensive investment banking experience responsible for leading Enterprise and Liquidity Risk across Mizuho EMEA. The role oversees the design and delivery of robust risk management frameworks ensuring compliance with evolving regulatory requirements an...
Enterprise And Liquidity Risk Managing Director
Mizuho
Profile SummaryA senior risk professional with extensive investment banking experience responsible for leading Enterprise and Liquidity Risk across Mizuho EMEA. The role oversees the design and delivery of robust risk management frameworks ensuring compliance with evolving regulatory requirements an...
Director, Translational Science Lead
Gsk
Director Translational Science LeadRenal Inflammation and Fibrosis and NeurodegenerationTranslational Sciences (TS) within Respiratory Immunology and Inflammation Research Unit (RIIRU) therapy area is accountable for end-to-end disease area translational science to inform therapy area and program le...
Director, Translational Science Lead
Gsk
Director Translational Science LeadRenal Inflammation and Fibrosis and NeurodegenerationTranslational Sciences (TS) within Respiratory Immunology and Inflammation Research Unit (RIIRU) therapy area is accountable for end-to-end disease area translational science to inform therapy area and program le...
Legal Counsel
Nato
OVERVIEW OF DIANANATO DIANA is the Defence Innovation Accelerator for the North Atlantic a NATO body dedicated to finding and accelerating innovation to provide decisive defence and security effects for the Alliance while fostering deep-tech innovation.NATO DIANA is comprised of a Board of Directors...
Associate Director, Global Clinical Physician
Bristol Myers Squibb
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...
Clinical Scientific Expert (cse) I
Novartis
Salary Range:37593.50 - 69816.50Job Description SummaryWork Arrangement: Hybrid Working #LI-HybridLocation: London (The Westworks) United KingdomRelocation Support: This role is based in London United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.ABOUT THE...
Method Developer Analyst
Syngenta Group
Are you a proactive problem solver with a passion for driving technical innovation Do you enjoy solving complex analytical problems and delivering innovative technical solutions We have an exciting opportunity for a Method Developer Analyst to join our Analytical Method & Metabolism (AMM) team and t...
Clinical Development Lead
Roche
At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...
(senior) Clinical Development Medical Director
Novartis
Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingLocation: London (The Westworks) United KingdomRelocation Support: This role is based in London United Kingdom. Please only apply if accessible.Are you passionate about shaping the future of clinical development and making a meaningful...
Associate Director, Cmc Regulatory Affairs (hemato...
Regeneron Pharmaceuticals
Build our future together:As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages mentor CMC Regulatory Affairs (RA) staff supporting cross-func...
Senior Regulatory Medical Writer
Fortrea
Sponsor-dedicated. Full time. Remote in the UK Spain South Africa Greece Portugal or Hungary.We are on a mission to deliver solutions that bring life-changing treatments to patients faster.But we cant do it alone. We are seeking an experienced Senior Regulatory Medical Writer to lead authoring and d...
Customs Regulatory Specialist
Fedex
GBR FedEx Express UK LimitedAddress:Endeavour House Coopers End RoadScheduled Weekly Hours:37.5Worker Type:RegularPosting Start Date9-Jun-2026Posting Close Date:15-Jun-2026Job Family:FXE-EU: Customs Regulatory Specialist (ID)Position Summary:An opportunity has come up within the Regulatory team.We b...
Medical Writer Ii, Oncology
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Sr Associate Regulatory Affairs Cmc
Amgen
Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATIONIf you feel like youre part of something bigger its because you are. At Amgen our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global col...