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Director, Regulatory Affairs Opthalmology

Job Description The Director of Regulatory Affairs will lead the regulatory function and play a central role in shaping and executing global regulatory strategies for our ophthalmology assets. Key Responsibilities Regulatory Leadership & Strategy Define and lead global regulatory strategy for ophthalmology programs from Phase II through Phase III and...

Trades Workforce Solutions

Horley

Quality & Regulatory Affairs Officer (UK MDR)

A UK-based consulting firm is seeking a Quality Assurance Officer to ensure compliance with medical device regulations in the UK and EU. This role involves managing the Quality Management System, conducting internal audits, and ensuring that documentation meets ISO 13485:2016 standards. The ideal candidate should have proven expertise in QA...

Wynne Consulting

Liverpool

Remote Regulatory Affairs Manager: EU CTR Strategy Lead

A leading global regulatory organization is seeking a Regulatory Affairs Manager to support the development and execution of global regulatory strategies for investigational submissions, particularly for EU and UK regulations. This remote role requires expertise in regulatory compliance, active collaboration with multidisciplinary teams, and the ability to manage complex regulatory...

Freyr Solutions

Leeds

Senior Regulatory Affairs Associate

Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world‑leading in vitro diagnostics company with award‑winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate...

QuidelOrtho

Bridgend

Senior Regulatory Affairs Strategist: Global Submissions Lead

A global clinical research organization is seeking an experienced Regulatory Affairs Professional to join as a Senior Regulatory Affairs Strategist in Uxbridge. The role, which can be home or office based, requires excellent leadership in regulatory negotiations and developing strategies for international submissions. Ideal candidates will have over 10 years...

Parexel

Uxbridge

International Regulatory Affairs Lead - Submissions & Strategy

A global pharmaceutical company is seeking an Associate Director of Regulatory Affairs to lead regulatory compliance for international markets. The role includes managing regulatory submissions, representing the regulatory team in launch activities, and collaborating across various functions. Candidates should have a BSc in relevant sciences and at least 10 years...

KalVista Pharmaceuticals

Salisbury

UK Regulatory Affairs Partner — MHRA Liaison (Hybrid)

A global pharmaceutical company in Welwyn Garden City is seeking a Regulatory Affairs Partner to leverage regulatory and scientific expertise. The role entails ensuring compliance with UK regulations while leading strategic initiatives. Applicants should hold a degree in Life Sciences and have extensive experience in UK Regulatory Affairs, including managing...

CK Group- Science, Clinical and Technical

Welwyn Garden City

EU Regulatory Affairs Lead for NPD & Compliance (Hybrid)

A leading healthcare company in Woking is seeking a Regulatory Affairs Manager to oversee regulatory activities for own-brand products. This hybrid role involves managing compliance and supporting new product development. The ideal candidate has a life science degree and experience in European regulatory affairs, coupled with strong communication and organizational...

Alliance Healthcare

Woking

Remote Regulatory Affairs Manager, Ecotoxicology (UK/EU)

A leading agrochemical company is seeking a Regulatory Affairs Manager as an independent consultant to manage ecotoxicology registrations in the UK. This role involves preparing registration dossiers, analyzing ecotoxicological studies, and leading projects while collaborating with various teams across Europe. Ideal candidates possess strong analytical skills and experience with UK...

Atrio Search

Leeds

UK Regulatory Affairs & Licensing Lead

A leading digital finance company in the United Kingdom is seeking an experienced professional for the Regulatory and Licensing team. This role involves engaging with regulators, monitoring regulatory developments, and managing relationships with various stakeholders. Candidates should have at least 5 years of experience in governmental or regulatory affairs, particularly...

Tether Operations Limited

City of London

Global Regulatory Affairs Manager: EU/UK CTA Strategy

A leading global Regulatory Solutions provider is looking for a Regulatory Affairs Manager to support the development and execution of global regulatory strategies for investigational submissions. This remote role focuses on ensuring compliance with EU and UK Clinical Trial Regulations. Responsibilities include managing submissions, collaborating with multidisciplinary teams, and ensuring...

Freyr Solutions

Sheffield

Global Regulatory Affairs Officer — Medical Devices

A leading organisation in healthcare is looking for a Regulatory Affairs Officer in Edinburgh. The successful candidate will develop regulatory strategies and manage product license registrations globally. Responsibilities include preparing regulatory documentation, advising teams on compliance, and maintaining ISO13485 standards. A relevant degree and experience in regulatory submissions within medical...

Edinburgh City Football Club Limited.

Edinburgh

European Regulatory Affairs Director, Strategy & Leadership

A global biopharmaceutical company is seeking a Regulatory Affairs Lead to define and implement regulatory strategies for their product portfolio in the Europe Region. The ideal candidate will have extensive experience in the pharmaceutical industry, particularly in regulatory affairs, and will demonstrate strong leadership capabilities, adept negotiation skills, and the...

AbbVie

Maidenhead

Remote Regulatory Affairs Training Manager — RIM (Veeva)

A leading life sciences consultancy is seeking a Regulatory Affairs Training Manager for an 18-month contract. The role focuses on developing and delivering training for the Veeva RIM system. Responsibilities include creating training materials, coordinating sessions for Super Users and End Users, and evaluating training effectiveness. Candidates should have a...

Cpl Life Sciences