Regulatory Affairs jobs in United Kingdom
Remote Global Regulatory Affairs Specialist Medical Devices
Rhian_Convatec
Global Regulatory Affairs VP: Lead Strategy & Inspections
Tokamak energy
EMEA Regulatory Affairs Expert – Biocides & REACH
STERIS
Global Regulatory Scientist: Submissions & Strategy
Syngenta
Docuvera Regulatory Specialist — Submissions & Compliance
Harrington Recruitment
Discover more opportunities than anywhere else. Find more jobs nowVeterinary Medicines Quality Assessor – Regulatory Authorisations
Veterinary Medicines Directorate (VMD)
Regulatory & Quality Lead - Medical Devices & ISO 13485
linkup
EU Regulatory Manager (Remote, 1-Year Contract)
BridgeBio
Connect with headhunters to apply for similar jobsHybrid Global Regulatory Compliance Specialist
The Beauty Tech Group
Global Regulatory Affairs Associate, Medical Devices (UK)
Resourcing Life Science
Regulatory Risk Manager – UK Regs & Strategy
PIC
Regulatory Affairs Specialist — Food & Feed (Hybrid)
Prinova Europe
Strategic Regulatory Affairs Project Manager - Europe
AbbVie
12-Month Regulatory Affairs Placement – Pharma
Takeda
Regulatory Affairs Specialist
Clifford Chance
Global Medical Affairs (Multiple Roles) Industrial Placement, UK 2026
WISE Campaign
Associate Director, Regulatory Affairs
Allergan
Regulatory Compliance & Incident Officer
Illumina, Inc
Medical Affairs Senior Advisor / Manager Vaccines & Infectious Diseases
Pfizer, S.A. de C.V
Medical Affairs Senior Advisor / Manager Vaccines & Infectious Diseases
Pfizer
Medical Affairs Senior Advisor / Manager Vaccines & Infectious Diseases
Pfizer
Global Clinical and Medical Affairs Manager
Creo Medical
Assistant Director of Government Relations: Penn Medicine
Bryn Mawr College
Remote Global Regulatory Affairs Specialist Medical Devices
Job summary
A leading medical technology company in the UK is seeking a Regulatory Affairs Specialist to ensure compliance of products within a defined group. Responsibilities include regulatory strategy development, writing and submitting regulatory dossiers, and managing global regulatory projects. The ideal candidate will have 1-2 years of experience in a regulatory role and a bachelor’s degree in a relevant field. This position is remote with occasional travel to the office in Deeside, UK.
Qualifications
- 1-2 years of relevant experience in regulatory affairs.
- Understanding of medical device regulatory framework.
- Experience with Class I, II, and III sterile medical devices.
Responsibilities
- Ensure regulatory compliance for a defined group of products.
- Write and submit regulatory dossiers and interface with authorities.
- Lead regulatory assessment for product changes.
Skills
Education
Tools
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.