Job Title: Senior Regulatory Affairs Officer Employment Type: Permanent Location: East London, 3 days on-site... per week. (Hybrid) Salary: Up to £50,000 Senior Regulatory Affairs Officer opportunity working for a growing pharmaceutical...
Cpl GroupJob Title: Senior Regulatory Affairs & PV Manager Employment Type: Permanent position Location: East London, 3 days... on site. (Hybrid) Remuneration: Competitive salary and package Senior Regulatory Affairs & PV Manager opportunity working...
Cpl Group. We currently have an exciting opportunity to join us as Senior Regulatory Manager, Clinical Affairs. The function of a Senior... of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations...
AbbottAffairs (Medical Devices). The successful candidate will be responsible for ensuring compliance with regulatory standards (MDD...We are seeking a meticulous and dedicated Senior Regulatory Affairs Associate with a strong background in Regulatory...
Michael Pagecompanies, including successful pre-market submissions. - Extensive knowledge of IVD medical device regulatory requirements...- Serve as Global Regulatory Science Lead in support of QIAGEN Translational Science and Precision Diagnostics (TSPDx...
Qiagencompanies, including successful pre-market submissions. - Extensive knowledge of IVD medical device regulatory requirements...- Serve as Global Regulatory Science Lead in support of QIAGEN Translational Science and Precision Diagnostics (TSPDx...
Qiagencompanies, including successful pre-market submissions. - Extensive knowledge of IVD medical device regulatory requirements...- Serve as Global Regulatory Science Lead in support of QIAGEN Translational Science and Precision Diagnostics (TSPDx...
Qiagencompanies, including successful pre-market submissions. - Extensive knowledge of IVD medical device regulatory requirements...- Serve as Global Regulatory Science Lead in support of QIAGEN Translational Science and Precision Diagnostics (TSPDx...
Qiagendevice or healthcare sector. Familiarity with regulatory compliance standards for medical devices, encompassing FDA... Assurance: Knowledge of regulatory requirements and quality assurance standards applicable to medical devices, including FDA...
Philipsfor you! Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role..., or Germany. Responsibilities: – Write and/or edit various clinical regulatory documents: As a Senior Regulatory Affairs...
NonStop Consultingand supply of medicines, medical devices, cosmetics, and other product categories. To formulate strategy and actions to assure.... To provide sound regulatory strategy and advice to support Senior Management within the business. Core responsibilities...
Mentholatum UK Ltdbusiness’s regulatory systems by maintaining and reporting our regulatory position to our senior management team. To act...Location : Holly Road - Skegness, United Kingdom Job Advert A Regulatory Officer vacancy has arisen in our fast...
MicroncleanExperience in Medical Devices and their clinical evaluation International Regulatory experience specifically USA Knowledge... of any future clinical development plans working closely with medical office and regulatory new products team to support the...
Lifelancer-growing group of companies within the medical devices sector is seeking a Group Director of Legal Services.... In this newly created role, you will support senior members of the legal team with a wide variety of legal issues...
Taylor RootJob Title Medical Robotics Senior Software Architect (Cambridge, MA) Job Description Medical Robotics Senior... devices and preferably for medical robots, as an individual contributor and a team lead with experience in robotic (HW/SW...
PhilipsJob Title Senior Software Architect - Medical Imaging Applications (Plymouth, MN) Job Description Senior Software... Architect - Medical Imaging Applications (Plymouth, MN) We are looking for: A highly skilled and experienced Senior Software...
PhilipsAt least 8 years’ experience of Life Sciences R&D, ideally within the fields of consumable medical devices At least 3 years... growth Understanding of global regulatory medical device requirements for new product introduction Experience in leading...
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