Regulatory Submissions Jobs in UK

 Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However the actual time you spend and where you spend it will vary by role or assignment including up to 5 days per week on a client site.This role can be based at either our London Victoria or Melb...

Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However the actual time you spend and where you spend it will vary by role or assignment including up to 5 days per week on a client site.This role can be based at either our London Victoria or Melbo...

DescriptionSenior Manager Regulatory AffairsAt Endomag a Hologic company we are driven by a clear purpose: advancing health through innovative medical technologies that improve and save lives. We are seeking an experienced Senior Manager Regulatory Affairs to lead the Regulatory function at our Camb...

DescriptionSenior Manager Regulatory AffairsAt Endomag a Hologic company we are driven by a clear purpose: advancing health through innovative medical technologies that improve and save lives. We are seeking an experienced Senior Manager Regulatory Affairs to lead the Regulatory function at our Camb...

Are you looking to join a company where your contributions truly matter and where youll be part of a supportive innovative teamMMS is aaward-winning data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization recognized for our exceptio...

Are you looking to join a company where your contributions truly matter and where youll be part of a supportive innovative teamMMS is aaward-winning data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization recognized for our exceptio...

JOB DESCRIPTION:Stats & Analysis ManagerWitney Site Based About AbbottAbbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medic...

Career CategoryOperationsJob 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...

Join IQVIA on our mission to accelerate innovation for a healthier world!We are seeking experienced Clinical Research Associates in Scotland to strengthen our cFSP sponsor-dedicated team.Why IQVIAWe share a passion for the work we do and the impact it has on customers and patients.We are innovative...

Job Title: Director Process Design and Optimisation in Chemical DevelopmentLocation: Macclesfield UKHybrid working model 3-5days per week onsiteAbout us:At AstraZenecawereunited by a bold ambition: to push the boundaries of science and deliver life-changing medicines to patients worldwide. As a glo...

Circa 40883(depending on skills & experience)2xPermanent /Full-time / 37 hours per week. (Flexible Working Opportunities available)RegionalRole (Baselocationcan be any Anglian Watermain officeor business hub (Huntingdon Peterborough LincolnNorwichor Colchester)Hybrid -(Minimum2days in office per wee...

Job Title: Medical Director Senior Patient Safety PhysicianLocation: 3 days onsite in Luton UK Are you ready to lead patient safety innovation at the forefront of global healthcareAt AstraZeneca were not just developing tomorrows medicineswere reimagining how patient safety shapes every breakthrough...

Title:CMC Lead Neurotoxins & BiologicsCompany: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...

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research development and manufacturing facility at Harwell to support ons...

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...

We 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 medicines and 409 million vaccine doses in 2024 to help make a positive impact on the h...

Make your mark for patientsWe are looking for a Global Regulatory Affairs CMC Lead who is collaborative strategic and delivery focused to join us in our Global Regulatory Affairs team based in any of our Brussels (Belgium) Slough (UK) or Atlanta/Raleigh (US) offices.About the roleYou will lead regul...

Make your mark for patientsWe are looking for a Regulatory CMC Scientist to join us in our Global Regulatory team based in any of our Brussels (Belgium) or Slough (UK) offices.About the roleDefine the strategy planning and preparation (writing and review) of CMC submission documentation for regulato...

Regulatory Affairs Manager London PermanentWe are looking for a Regulatory Affairs Manager to focus on how works with its regulators across the UK payments landscape. This role suits an experienced regulatory or policy professional who wants clarity of scope defined responsibilities and meaningful...

Assytem is recruiting two experienced Technical Quality Document Management (TQDM) Specialists to support a high-profile client operating within a highly regulated engineering environment.This opportunity is ideal for professionals with 5 years experience in document control information management o...