Latest Regulatory Affairs Specialist Jobs

Global Regulatory Affairs Manager — Hybrid (3 days in-office)

A global healthcare company is seeking a Regulatory Affairs Manager to join their team in Hampshire, UK. This full-time role focuses on managing complex global projects and submissions within the realm of European Medicinal Regulatory Affairs. The successful candidate will lead regulatory activities, collaborate with cross-functional teams, and interact with...

Alimera

Hook

Graduate Regulatory Affairs Associate — Hybrid UK

A leading regulatory consultancy in Letchworth is looking for a Regulatory Affairs Associate. This entry-level role is perfect for recent graduates and involves supporting cross-functional teams and regulatory projects. Candidates should hold a Life Science or Pharmacy Degree and be fluent in English. The position starts onsite during the probation...

DLRC Regulatory Consultancy

Letchworth Garden City

Global Regulatory Affairs Lead – Medical Devices

A leading technology firm in the United Kingdom is seeking a Regulatory Affairs Manager to oversee regulatory clearances in global markets. The ideal candidate will have over 5 years of compliance experience in the medical device sector and a strong knowledge of EU and FDA regulations. This role offers an...

Vicon

Yarnton

Remote Regulatory Affairs Leader — Biotech Innovations

A global biotechnology company based in Uxbridge is seeking an experienced Regulatory Affairs Manager to ensure proper licenses for clinical trials and marketing products. The role involves managing regulatory submissions, providing guidance on regional regulations, and working with a team on product strategy. Ideal candidates will have a scientific degree...

Amgen

Uxbridge

Regulatory Lead - Medical Devices, Cosmetics & Supplements

A leading healthcare company is hiring a Regulatory Affairs Manager in Huddersfield. This exciting role involves managing regulatory activities for medical devices, cosmetics, and food supplements while ensuring compliance with UK and EU regulations. Candidates should possess at least 5 years of experience in regulatory affairs and a relevant degree....

tendersglobal

Huddersfield

Director CMC Regulatory Affairs

Responsibilities: Lead global CMC regulatory strategy for commercial biologic products, focusing on post-approval changes, lifecycle management, and dossier maintenance.Prepare and deliver high-quality CMC documentation for global submissions (e.g., supplements, variations, amendments) supporting manufacturing process changes, analytical method updates, site changes, and supplier modifications.Provide strategic guidance to cross-functional teams based on...

Discover International

Nottingham

Director CMC Regulatory Affairs

Responsibilities: Lead global CMC regulatory strategy for commercial biologic products, focusing on post-approval changes, lifecycle management, and dossier maintenance.Prepare and deliver high-quality CMC documentation for global submissions (e.g., supplements, variations, amendments) supporting manufacturing process changes, analytical method updates, site changes, and supplier modifications.Provide strategic guidance to cross-functional teams based on...

Discover International

Newcastle upon Tyne

Director CMC Regulatory Affairs

Responsibilities: Lead global CMC regulatory strategy for commercial biologic products, focusing on post-approval changes, lifecycle management, and dossier maintenance.Prepare and deliver high-quality CMC documentation for global submissions (e.g., supplements, variations, amendments) supporting manufacturing process changes, analytical method updates, site changes, and supplier modifications.Provide strategic guidance to cross-functional teams based on...

Discover International

Sheffield

EU Senior Regulatory Affairs Manager / FTC

Job Title: EU Regulatory Affairs Manager Department: Regulatory Affairs Location: Uxbridge, UK or Dublin, Ireland – 3x a week in the office Job Type: 12 Month Contract /FTC Remuneration: Up to £85,000/€90,000 This is a 12-month contract role, and you MUST be able to start this role within 4 weeks....

Cpl Life Sciences

Uxbridge

Director CMC Regulatory Affairs

Responsibilities: Lead global CMC regulatory strategy for commercial biologic products, focusing on post-approval changes, lifecycle management, and dossier maintenance.Prepare and deliver high-quality CMC documentation for global submissions (e.g., supplements, variations, amendments) supporting manufacturing process changes, analytical method updates, site changes, and supplier modifications.Provide strategic guidance to cross-functional teams based on...

Discover International

Leeds

Director CMC Regulatory Affairs

Responsibilities: Lead global CMC regulatory strategy for commercial biologic products, focusing on post-approval changes, lifecycle management, and dossier maintenance.Prepare and deliver high-quality CMC documentation for global submissions (e.g., supplements, variations, amendments) supporting manufacturing process changes, analytical method updates, site changes, and supplier modifications.Provide strategic guidance to cross-functional teams based on...

Discover International

Birmingham

Director CMC Regulatory Affairs

Responsibilities: Lead global CMC regulatory strategy for commercial biologic products, focusing on post-approval changes, lifecycle management, and dossier maintenance.Prepare and deliver high-quality CMC documentation for global submissions (e.g., supplements, variations, amendments) supporting manufacturing process changes, analytical method updates, site changes, and supplier modifications.Provide strategic guidance to cross-functional teams based on...

Discover International

Manchester

Director CMC Regulatory Affairs

Responsibilities: Lead global CMC regulatory strategy for commercial biologic products, focusing on post-approval changes, lifecycle management, and dossier maintenance.Prepare and deliver high-quality CMC documentation for global submissions (e.g., supplements, variations, amendments) supporting manufacturing process changes, analytical method updates, site changes, and supplier modifications.Provide strategic guidance to cross-functional teams based on...

Discover International

Bristol

Director CMC Regulatory Affairs

Responsibilities: Lead global CMC regulatory strategy for commercial biologic products, focusing on post-approval changes, lifecycle management, and dossier maintenance.Prepare and deliver high-quality CMC documentation for global submissions (e.g., supplements, variations, amendments) supporting manufacturing process changes, analytical method updates, site changes, and supplier modifications.Provide strategic guidance to cross-functional teams based on...

Discover International

Glasgow

Director CMC Regulatory Affairs

Responsibilities: Lead global CMC regulatory strategy for commercial biologic products, focusing on post-approval changes, lifecycle management, and dossier maintenance.Prepare and deliver high-quality CMC documentation for global submissions (e.g., supplements, variations, amendments) supporting manufacturing process changes, analytical method updates, site changes, and supplier modifications.Provide strategic guidance to cross-functional teams based on...

Discover International

London