Latest Data Scientist (Healthcare) Jobs

Manufacturing Engineer

Manufacturing Engineer Join a leading manufacturer of high-specification components and materials for the medical sector, where precision, innovation, and problem-solving are at the heart of everything they do. They're looking for a proactive Manufacturing Engineer who’s excited to support advanced medical-grade production and drive continuous improvement across operations. What You’ll...

Zenith Advisory Partners

Bacup

Senior Quality Engineer

Senior Quality Engineer £40,000 - £50,000 DOE Tewksbury Are you an experienced quality professional with a passion for ensuring excellence in manufacturing environments? We are recruiting a Senior Quality Engineer to join a dynamic team dedicated to delivering top-tier, fully compliant products in a high-reliability industry. Key Responsibilities: Lead and...

Orion Electrotech

Tewkesbury

Procurement Specialist

Are you looking for a fantastic opportunity to work for a progressive medical technology company? Do you have experience with dealing with goods? If so, read on… Our client is among the world's leading suppliers of medical devices and a leading innovator . They offer a warm and friendly working...

Randstad Inhouse Services

Plymouth

Bioelectronics Engineer

CK Group are recruiting for a Bioelectronics Engineer to join a biotechnology start-up based in Cambridge on a permanent basis. The Company: Our client are engineering a scalable, end-to-end Cultured Meat production system, including bioprocesses, enabling technologies, software, hardware and raw materials to empower food producers all over the world...

CK Group- Science, Clinical and Technical

Cambridge

Regulatory Affairs Associate

Job ref: RAA11225 Job type: Permanent Location: Newry Closing date: Monday 05 Jan 2026 13:00 Job Overview To assist in registration and maintenance of Veterinary Medicinal Products in the US and Canadian Markets Main Activities/Tasks The compilation of regulatory applications for submission to the US FDA and Canadian Authorities and...

Norbrook

Newry

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 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

City of 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

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