Regulatory Affairs jobs
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Found 156 jobs
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Manager / Senior Associate Regulatory Affairs CMC
A career within Gilead’s lean, fast paced regulatory team will give you the opportunity to grow your experience quickly. Working with an experience...
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Head of Quality and Regulatory Affairs
Ihr Aufgabengebiet: Beauftragter der obersten Leitung / Qualitätsmanagementbeauftragter gem. EN ISO 13485:2016 Person Responsible For Regulatory ...
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Associate Director / Manager, Global Regulatory Affairs
We have a fantastic opportunity for a talented Global Regulatory Affairs Associate Director/ Manager.
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Senior Director, Global Regulatory Affairs - Europe, Middle East, Africa, Asia-Pacific
This role encompasses responsibilities for Regulatory Affairs in Europe (western and eastern), Middle East, Africa, and Asia-Pacific geographie
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Senior Associate Regulatory Affairs
CK Group are recruiting for a Senior Associate Regulatory Affairs to join a biopharmaceutical company at their site based in Uxbridge on a contract...
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Regulatory Affairs Senior Manager
CK Group are recruiting for a Regulatory Affairs Senior Manager to join a biopharmaceutical company at their site based in Uxbridge on a contract b...
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Regulatory Affairs Specialist - Netherlands
New opportunity for a Regulatory Affairs Specialist (Junior/Senior) to work for an exciting biotech company in the south of the Netherlands
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QARA Contractor
My Client, an award winning start up company in the UK, are seeking a QARA Contractor to work with them on a 12 month interim project.
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Global Labelling Lead - UK
Regulatory Affairs - Global Labelling Lead - Pharmaceutical Industry.This is a 12 month freelance contract. UK - Reading - Office Base once COVID rest
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Senior Regulatory Affairs Associate
Senior Associate Regulatory Affairs12 Month Contract1.0 FTEUxbridge - UK Please note International relocations will not be considered for this role Jo
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Senior Regulatory Affairs Manager
Senior Manager - Regulatory Affairs 12 Month Contract Applicants MUST be based in the UK already, you will not be considered should you wish to reloca
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Senior Scientific Specialist - Medcomms
Senior Scientific Specialist Scientific and Editorial Services MedCom Act as senior therapy area/content expert and lead the delivery of assigned pro
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Junior Document Review Specialist - Freelance - Ghent, Belgium
i-Pharm Consulting is seeking on behalf of a Top Global CRO Freelance Junior Document Review Specialist. This is a home-based role however will requir
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Senior Regulatory Affairs Consultant - Home based / Office split
To apply for this role please call Julie Cooper on 07951 082482. Alternatively please send your CV to: julie@mosaicrecruitment.co.uk
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Senior Regulatory Affairs Consultant - NEW ROLE- Do you have European Product launch experience?
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or email your CV in confidence to :julie@mosaicrecruitment
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Reg Affairs Consultant - Medical Devices / Combination products- Remote - knowledge of CER/MDD/MDR
Medical Device Regulatory Consultant Medical Device Regulatory Consultant This company is looking for a Medical Device Subject Matter Expert based ...
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Risk Management Specialist
Risk Management Specialist (Class 1 Medical Device) based in Hamburg (25% onsite) on a freelance basis. 1 FTE for 3 -6 months.
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Regulatory Affairs Manager, Development & Strategy / Orphan Drugs/PIPs/Scientific Advice
Regulatory Manager; Development & Strategy; Biopharma; Biologics & Pharma Products; Central/West London
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Head of Labelling / Regulatory Affairs, Europe
European Labelling Lead; Team Manager & Project Lead; Labelling Subject Matter Expert; Significant salary package; Hertfordshire location
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Regulatory Affairs Manager
UK based Pharmaceutical Manufacturer and R&D Laboratory seeks a Regulatory Affairs Manager.
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