Medical devices regulatory affairs jobs in Potters Bar

Up to £50,000 Senior Regulatory Affairs Officer opportunity working for a growing pharmaceutical company that specialising in medicinal, non-medicinal, medical devices, and OTC products. The ...

Competitive salary and package Senior Regulatory Affairs & PV Manager opportunity working for a growing pharmaceutical company specialising in medicinal, non-medicinal, medical devices, and OTC ...

... medical products. * Contributing regulatory guidance in order to enhance product development ... Previous experience in Regulatory Affairs and Compliance particularly within pharmaceutical ...

... high medical needs of rare disease patients and providing treatment and services to them. Our ... The Manager, Regulatory Affairs International supports our ambitious geographical expansion plans

Medical Diagnostics Design Engineer - Electromechanical Design - London A new Medical Devices start ... Regulatory Affairs, Quality Assurance, and Field Service Engineering sectors.

... devices. * Tech - working across some of the most exciting tech policy areas, including ... At least 3 years' experience gained from working in consultancy, in-house, thinktank, regulator or ...

Technical background within software medical devices with a strong understanding of the regulatory function, and a good knowledge of related quality, engineering, clinical, safety, and post-market ...

Bachelor's degree in a relevant field (e.g., Engineering, Life Sciences, Regulatory Affairs) * 2 years' experience in quality and regulatory affairs within the medical device industry, preferably ...

Pharmaceutical industry (medical information, medical communication, medical affairs, safety, regulatory) experience would be preferable. Freshers with lab work/ research/PharmD background can be ...

... affairs, meetings, and HCP and patient education. They cover a variety of therapy areas including ... In depth knowledge of the pharmaceutical industry and associated regulations. * Superb relationship ...

Health-care regulatory body Do you have an interest in politics and current affairs is so this ... high standards in medical education and practise. Apply now to be part of a dynamic and ...

... medical devices as well as an understanding of how and why the devices can support healthcare delivery. * Extensive knowledge of medical device standards safety regulations pertaining to their ...

... Medical Device, IMP management, Regulatory Affairs and Pharmacovigilance · Experience in Monitoring, Quality Assurance and/or Good Clinical Practices · Exposure to inspections COMPETENCIES · ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Health-care regulatory body Do you have an interest in politics and current affairs is so this ... high standards in medical education and practise. Apply now to be part of a dynamic and ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Collaborates with local medical affairs colleagues on country specific studies and initiatives * Provides knowledge and expertise on country specific regulations and site experience and suitability ...

... Regulatory Affairs, Clinical Development, Medical Affairs and Quality Assurance - all functions are booming and there is a real demand in the US for international talent to support the market. The ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Responsibilities: • Conduct Human Factors studies to assess the usability of medical devices ... Create regulatory paperwork such as human factors summary reports, threshold analyses, and ...

From orchestrating on-site meetings, congresses, and symposia to developing medical affairs content ... Familiarity with ABPI regulations. * Experience with Veeva, Promomats and CRM platforms. 🎁 ...

Partnering with Medical Affairs, Marketing, and Commercial groups, you will provide market access ... regulations, health technology assessments, and determine implications alongside internal ...

... regulatory matters within the life sciences realm, especially concerning the supervision of medical devices, pharmaceuticals, cutting-edge technologies, and AI application, would be beneficial