Regulatory Affairs Manager

Regulatory Affairs manager – Medical DevicesOverviewRegulatory Affairs manager – Medical Devices. A new role in Regulatory Affairs has become available at an exciting medical devices organisation with products undergoing clinical trials. The role focuses on FDA and UK/EU submissions.The candidate will manage and prepare regulatory submissions (e.g.,...

Job DescriptionThe Regulatory Affairs Manager is responsible for managing new and existing regulatory clearances in global markets, including the EU, UK, USA, and globally through support of a distribution network.Plan and achieve medical device regulatory submission activities including new market applications, registrations, and renewals. Act as an...

The Regulatory Affairs Manager is responsible for managing new and existing regulatory clearances in global markets, including the EU, UK, USA, and globally through support of a distribution network.Is your CV ready If so, and you are confident this is the role for you, make sure to apply asap.Plan and achieve medical device regulatory submission activities...

Ready to lead global regulatory strategy? Want to shape compliance for innovative medical technologies? Looking for flexibility, ownership, and international impact? A forward-thinking medical device company is seeking a Regulatory Affairs Manager to join its Quality and Compliance function, playing a pivotal role in managing global regulatory approvals...

Regulatory Affairs ManagerRead on to find out what you will need to succeed in this position, including skills, qualifications, and experience.Department: Vicon Quality & Regulatory ComplianceEmployment Type: Permanent - Full TimeLocation: Yarnton, OxfordshireReporting To: Adam TaylorDescriptionAre you interested in working on products at the very cutting...

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world's largest RCO (Research Consulting Organization),...

Role OverviewAn exciting opportunity for a VP, Global Regulatory Affairs to join a leading Cell and Gene Therapy CDMO. As the VP, Global Regulatory Affairs, you will play a key role in providing global regulatory leadership, supporting clients developing advanced therapy programmes from early development through to commercialisation.You will be responsible...

**About Mirada Medical...** Mirada Medical develops medical imaging and cancer treatment planning solutions that provide simple and accessible solutions to complex image analysis problems in the diagnosis and treatment of cancer and other diseases. Our solutions interoperate with other IT systems in the healthcare enterprise, such as EHRs and PACS,...

Quality Assurance Regulatory Affairs Manager Cure Talent is partnered with an innovative medical device company developing novel technology ahead of a planned U.S. launch in 2028. As the company prepares for significant regulatory milestones, we have an exciting opportunity for a Regulatory Affairs & Quality Assurance Manager to join their growing team. In...

Are you an experienced Regulatory Affairs Specialist looking for your next role in an exciting new team? **About the Role** Day to day you will assist in correspondence with review agencies, notified bodies, and trade associations on matters relating to product registrations and PMS. You will liaise with other departments on all cross-functional teams...