Latest Product Manager (MedTech) Jobs

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

Newcastle upon Tyne

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

Bristol

Head of Scientific and Regulatory Affairs

Head of Scientific and Regulatory Affairs Be among the first 25 applicants. a US-headquartered Fortune 500 provider of ingredient solutions that helps nourish, comfort, sustain, and delight people around the world. Our wide range of ingredient solutions is strategically designed to address changing consumer trends and preferences. Our portfolio includes...

Kanz

Manchester

Regulatory Affairs Specialist - Medical Devices (Hybrid)

A financial services company is seeking a Regulatory Affairs Specialist to manage regulatory submissions and compliance for advanced wound care products. The role requires a background in life sciences and experience with medical device regulations. Strong organizational and relationship-building skills are essential. You will have access to a hybrid working...

Eagleston Financial Group

Hull

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

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

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

Senior Mechanical Design Engineer

Senior Design Engineer An established engineering and manufacturing business based in Portsmouth is looking for a Senior Design Engineer who can take the lead on turning ideas into practical, safe and reliable products. You’ll be involved in every stage of the design journey, shaping concepts, developing detailed technical work, supporting...

Altera Recruitment Group Ltd

Portsmouth