Latest Quality Assurance (MedTech) Jobs

Toolmaker

Toolmaker Permanent £18.00 - £20.00 per hour Days – Flexible hours! Redditch Our client is a trusted UK manufacturer of high-quality medical devices, recognised globally for precision engineering, innovation and consistent product excellence. With a long-established heritage supporting the healthcare sector, their operation is built around accuracy, cleanliness and uncompromising...

YG Engineering Ltd

Redditch

Regulatory Affairs Specialist

Regulatory Affairs Specialist Location: Buckinghamshire Salary: £40,000-£55,000 (dependent on experience) Our client is an established life sciences business based in Buckinghamshire. They distribute and manufacture high-quality and innovative products, including in-vitro diagnostics, laboratory reagents, and biological materials, across the European life sciences market. An opportunity has become available for an...

Taylorollinson

Buckingham

Medical Device Embedded Software Engineer

Talent STEM are working with an innovative medical device organisation that is expanding its embedded software capability and seeking an Experienced Embedded Software Engineer to join a growing technical team. This role offers the chance to work on complex, high-reliability medical systems in a highly regulated, quality-driven environment. You will...

Talent STEM Ltd

Littlemore

Production Manager

Futures Recruitment are looking to appoint a Production Manager to lead end-to-end manufacturing operations within a high-value, low-volume production environment. This role is critical to delivering bespoke, products where quality, reliability, and attention to detail are paramount. The ideal candidate will combine strong operational leadership with a deep understanding of...

Permanent Futures Limited

Holme Chapel

Manufacturing and Testing Assistant

Opportunity: Manufacturing & Testing Assistant (Medical Devices) Are you detail-oriented, reliable, and passionate about quality? Join our team in B15 1QT and play a crucial part in the production and testing of essential medical devices! Location B15 1QT Pay Rate £12.65 per hour Hours Full-Time: 8:00 AM - 4:30 PM,...

Randstad Engineering

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

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

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

Liverpool

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