REGULATORY AFFAIRS SPECIALIST jobs in SOUTH EAST, United Kingdom

Senior Regulatory Affairs Specialist - Medical Devices & IVD's Oxfordshire, UK - Office based Up... business currently has one open positions as a Senior Regulatory Affairs Specialist who will be responsible for planning...

Regulatory Affairs Specialist, RA Specialist, FDA, 510(K), SaMD, Remote, COR5716 The Role This is an excellent... Regulatory Affairs Specialist / RA Specialist, working for a company with a growing reputation in their field. The...

Reference Number: JO-2406-536433 Senior Regulatory Affairs Specialist Rate: £58,000 – 60,500 Job Type: Permanent... Location: Oxford Senior Regulatory Affairs Specialist – Medical Devices & IVD’s Oxfordshire, UK – Office based Up...

Regulatory Affairs Specialist Salary: Attractive, with excellent benefits Location: Bishops Stortford, Essex/Herts... Border A global medical device company seeks a Regulatory Affairs Specialist to ensure compliance across its global...

from strength to strength in recent years and are now looking for a Regulatory Affairs Specialist to join their expert team. In...An excellent role on offer for an individual with strong regulatory affairs experience within the medical device sector...

Specialist Regulatory Affairs in Advertising & Promotional materials Location: Witney (Primary) / Maidenhead... Specialist Regulatory Affairs, Advertising & Promotion, combines scientific, regulatory, and business expertise to ensure...

a Senior Regulatory Affairs Specialist to join the EMEAP regulatory affairs team, which is growing to meet the demands of the... and significant on-market changes for the Europe, Middle East and Africa (EMEA) region. You will work with the Regulatory Affairs...

Registration & Regulatory Affairs BPR (Biocidal Product Registration) Specialist Location: Frimley, UK Function...: GSARA (global safety assessment and regulatory affairs) About the role The Global Registration and Regulatory...

Regulatory Affairs Specialist, RA Specialist, FDA, 510(K), SaMD, Remote, COR5716 The Role This is an excellent... Regulatory Affairs Specialist / RA Specialist, working for a company with a growing reputation in their field. The...

Zest Scientific is actively recruiting for a Senior Regulatory Specialist in the field of medical devices for a leading... medical devices industry (coupled with some work in the pharmaceutical sector), you will leverage your regulatory knowledge...

of Regulatory & Clinical Affairs to be based in the UK. You will be leading an experienced team of regulatory and clinical... professionals, working strategically whilst remaining operational to spearhead regulatory strategy development and drive regulatory...

of Regulatory & Clinical Affairs to be based in the UK. You will be leading an experienced team of regulatory and clinical... professionals, working strategically whilst remaining operational to spearhead regulatory strategy development and drive regulatory...

Job Title: Senior Regulatory Affairs Specialist Employment Type: Permanent, Full time Location: Kent UK, 3 days... on-site per week. (Hybrid) Salary: Up to £55,000 Senior Regulatory Affairs Specialist opportunity working for a growing...

Location: Sandwich Job Title: Senior Regulatory Affairs Specialist Employment Type: Permanent, Full time Location: Kent... UK, 3 days on-site per week. (Hybrid) Salary: Up to £55,000 Senior Regulatory Affairs Specialist opportunity working...

a Senior Regulatory Affairs Specialist to join the EMEAP regulatory affairs team, which is growing to meet the demands of the... and significant on-market changes for the Europe, Middle East and Africa (EMEA) region. You will work with the Regulatory Affairs...

, and commercialization activities within Regulatory Affairs. Ability to understand, assess and manage the regulatory implications of product...Proclinical is seeking a dedicated and detail-oriented Regulatory Labelling Manager. The successful candidate...

strategic thinking, excellent communication skills, and a strong understanding of regulatory affairs. Please note... of labelling within a therapeutic area. Experience in regulatory affairs, safety, scientific, or medical writing. Direct...