Jobs in London

Regulatory Affairs Specialist

CK Group are recruiting for a Regulatory Affairs Specialist to join a fast growing software platform that is simplifying global product compliance. This role will be based in London on a permanent basis. Company: The client manage a number of regulatory products designed to support regulatory compliance. Location: The role...

CK Group- Science, Clinical and Technical

London

Senior Development Engineer - Drug Delivery Devices

Senior Development Engineer - Drug Delivery Devices Newton Colmore is partnered with a start-up medical devices company in London and we are helping them find a development engineer to join their research team. As a Development Engineer in this company, you will be working on a novel injectable drug delivery...

Newton Colmore

London

Recruitment

Recruitment Consultant – Life Sciences London (Hybrid: 3 Days in Office) Our client is a growing and highly regarded recruitment business specialising in the life sciences sector, working with organisations across pharmaceuticals, biotechnology, medical devices, and clinical research. Due to continued expansion, they are hiring Recruitment Consultants to join their...

Aspire Rec2Rec

London

Product Specialist

The Company:  Market leading distributor within the medical devices industry.  Incredible training/coaching.  Family run business and agile so can make decisions quickly.   Benefits of the Product Specialist  £30k basic    Commission paid monthly (Genuine opportunity to earn £40k+ in addition to basic salary & Uncapped)  Company Car   Healthcare   Pension   Mobile   Laptop  ...

On Target Recruitment Ltd

London

Regulatory Affairs Specialist (Food Ingredients)

Our client: A global leader in ingredient solutions, supporting innovation across food, beverage, and nutrition markets.Driving growth through strategic partnerships with retailers, manufacturers, and health-focused brands.Renowned for high-quality, functional ingredients that help brands meet evolving consumer needs. The role: The Regulatory Affairs Specialist will ensure full compliance with UK, EU,...

Seven Search and Selection Ltd

London

Business Development Manager - Medical Devices (mobility equipment)

Business Development Manager - Medical Devices (Mobility Equipment) OTE £55k-£67.5k (uncapped)Vehicle + benefitsNorth West England A leading medical equipment manufacturer is looking for a BDM within the Mobility & Specialist Rehab Territory to grow their wheelchair and specialist seating portfolio across the North West. This is a field-based commercial role...

Identify Solutions

London

CLINICAL SPECIALIST – Structural Medical Devices

CLINICAL SPECIALIST – Cardiology Medical Devices Permanent opportunity London/Greater London area Are you someone who enjoys educating medical teams and conducting training sessions? Do you enjoy travelling and meeting different surgeons and hospital? Our client provides cutting-edge medical devices, coupled with unparalleled support to healthcare professionals. If you come from...

PROJECTUS

London

Clinical Trials Supply Chain Manager

Our client, a global pharmaceutical company, is currently looking for a Clinical Trials Supply Chain Manager to join their team in Uxbridge on a full time, 6-month temporary basis (35 hours per week). This role is expected to be worked on a hybrid basis but remote applications will also be...

Park Street People

London

Lead Clinical Trials Pharmacist

Who are we? Clerkenwell Health is an innovative and leading Research Organisation specialising in the delivery of scientifically grounded clinical trials through its collaborative Contract Research Organisation, extensive Site Network and pioneering Therapy Development Programme. We focus on advancing Mental Health and CNS research, with particular expertise in supporting psychedelic...

Clerkenwell Health

London

Regulatory Affairs Manager

My client is looking for a Regulatory Affairs Manager (Independent Consultant) to strengthen its European regulatory affairs team and support the registration of plant protection products in the United Kingdom. Mission 1 – Manage UK Ecotoxicology Registrations Prepare, submit, and maintain registration dossiers for plant protection products under the UK...

Atrio Search

London

Regulatory Affairs Coordinator

We are a global luxury skincare company known for our science-backed products that deliver proven results. Founded with a purpose, we remain deeply committed to innovation, sustainability, and excellence in everything we do. As we continue to grow, our fast-paced environment is rooted in collaboration, kindness, and a family-like culture...

Augustinus Bader

London

Regulatory Affairs Director

Regulatory Affairs Director Our client is a young exciting publicly listed clinical-stage company dedicated to transforming the lives of patients in its therapy areas. With its novel and proprietary drug products and current clinical development programs our client is aiming to provide improved treatments for patients with increased remission rates,...

The RFT Group

London

Senior Regulatory Affairs Specialist

🔬 Join a Dynamic Regulatory Team in the Crop Protection Industry! The Client: For over thirty years, our client, an Irish-owned family firm, has been a trusted supplier of plant protection products. They are keen on making sure their customers have a good experience all round, building proper long-lasting relationships,...

Amicus Search & Recruitment

London

Freelance/Contract Regulatory Affairs Project Manager - Clinical trial applications (CTA's)

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma...

ProPharma

London

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