cmc regulatory contractor jobs

A biopharmaceutical company in the UK seeks an experienced Associate Director, Regulatory Affairs CMC, responsible for leading global CMC regulatory strategies for its innovative cell and gene therapy products. The ideal candidate will have 8-10 years of experience in Regulatory Affairs for biologics, excellent communication skills, and a proven track record in regulatory submissions and...

The (Associate) Director, Post-Market Regulatory CMC will lead lifecycle CMC regulatory strategy and execution for commercial Advanced Therapy Medicinal Products (ATMPs), biologics, and oncology products. This role supports global regulatory compliance, manages post-approval changes, and drives high-quality submissions to ensure product availability for patients. Key Responsibilities Regulatory...

You will work cross-functionally with internal teams and external partners to ensure timely and compliant submissions to EMA and national authorities. Key Responsibilities: - Lead regulatory strategy development for new and existing products, including De-centralised/orphan and generic submissions.

Manager, CMC Process Development Location: Manchester (Fully Site‑Based) Hours: 7:00am – 3:00pm, Mon-Fri Contract: Permanent Reports to: Head of Validation UK About the Role We are seeking an experienced Manager, CMC Process Development to lead the transition of new pharmaceutical products from early research through scale‑up and into GMP manufacturing. This is a highly specialised,...

Contract Length: 12 months Workload: 20 hours/week Location: UK-based role Start Date: February Engagement: B2B Role Overview: We are seeking an experienced CMC leader to drive Chemistry, Manufacturing & Controls (CMC) activities for the late-stage clinical development of a novel Fc-fusion protein targeting NT-3 for chronic pain and osteoarthritis. This role will focus on ensuring...

Accession Therapeutics Limited, a vibrant clinical-phase company based on the ARC Oxford site, is looking for a Senior Scientist to join the Process Development section of its CMC group; this is a fixed-term (12 months) post to cover a period of maternity leave. We are looking for candidates who are able to : · Support the company's ATMP/ biologics process development (downstream)...

Accession Therapeutics Limited, a vibrant clinical-phase company based on the ARC Oxford site, is looking for a Senior Scientist to join the Process Development section of its CMC group; this is a fixed-term (12 months) post to cover a period of maternity leave. We are looking for candidates who are able to : · Support the company's ATMP/ biologics process development (downstream)...

Manager, CMC Process DevelopmentLocation: Manchester (Fully Site‑Based)Hours: 7:00am – 3:00pm, Mon-FriContract: PermanentReports to: Head of Validation UKAbout the RoleWe are seeking an experienced Manager, CMC Process Development to lead the transition of new pharmaceutical products from early research through scale‑up and into GMP manufacturing.This is a highly specialised, independent role at...

The (Associate) Director, Post-Market Regulatory CMC will lead lifecycle CMC regulatory strategy and execution for commercial Advanced Therapy Medicinal Products (ATMPs), biologics, and oncology products. This role supports global regulatory compliance, manages post-approval changes, and drives high-quality submissions to ensure product availability for patients. Key ResponsibilitiesRegulatory...

(Associate) Director, Regulatory Affairs CMC page is loaded## (Associate) Director, Regulatory Affairs CMClocations: UK - London, White City: UK - Stevenagetime type: Full timeposted on: Posted Todaytime left to apply: End Date: March 27, 2026 (30+ days left to apply)job requisition id: JR100066**Work with us** Our team are passionate in the pursuit of excellence and in pushing the boundaries of...

Accession Therapeutics Limited, a vibrant clinical-phase company based on the ARC Oxford site, is looking for a Senior Scientist to join the Process Development section of its CMC group; this is a fixed-term (12 months) post to cover a period of maternity leave. We are looking for candidates who are able to :· Support the company's ATMP/ biologics process development (downstream) capabilities ·...

You will work cross-functionally with internal teams and external partners to ensure timely and compliant submissions to EMA and national authorities. Key Responsibilities: - Lead regulatory strategy development for new and existing products, including De-centralised/orphan and generic submissions.

You will work cross-functionally with internal teams and external partners to ensure timely and compliant submissions to EMA and national authorities. Key Responsibilities: - Lead regulatory strategy development for new and existing products, including De-centralised/orphan and generic submissions.

The (Associate) Director, Post-Market Regulatory CMC will lead lifecycle CMC regulatory strategy and execution for commercial Advanced Therapy Medicinal Products (ATMPs), biologics, and oncology products. This role supports global regulatory compliance, manages post-approval changes, and drives high-quality submissions to ensure product availability for patients. Key ResponsibilitiesRegulatory...

You will work cross-functionally with internal teams and external partners to ensure timely and compliant submissions to EMA and national authorities. Key Responsibilities: - Lead regulatory strategy development for new and existing products, including De-centralised/orphan and generic submissions.

The (Associate) Director, Post-Market Regulatory CMC will lead lifecycle CMC regulatory strategy and execution for commercial Advanced Therapy Medicinal Products (ATMPs), biologics, and oncology products. This role supports global regulatory compliance, manages post-approval changes, and drives high-quality submissions to ensure product availability for patients. Key ResponsibilitiesRegulatory...

The (Associate) Director, Post-Market Regulatory CMC will lead lifecycle CMC regulatory strategy and execution for commercial Advanced Therapy Medicinal Products (ATMPs), biologics, and oncology products. This role supports global regulatory compliance, manages post-approval changes, and drives high-quality submissions to ensure product availability for patients. Key ResponsibilitiesRegulatory...

Contract Length: 12 monthsWorkload: 20 hours/weekLocation: UK-based roleStart Date: February Engagement: B2BRole Overview:We are seeking an experienced CMC leader to drive Chemistry, Manufacturing & Controls (CMC) activities for the late-stage clinical development of a novel Fc-fusion protein targeting NT-3 for chronic pain and osteoarthritis. This role will focus on ensuring readiness for large,...

Contract Length: 12 monthsWorkload: 20 hours/weekLocation: UK-based roleStart Date: February Engagement: B2BRole Overview:We are seeking an experienced CMC leader to drive Chemistry, Manufacturing & Controls (CMC) activities for the late-stage clinical development of a novel Fc-fusion protein targeting NT-3 for chronic pain and osteoarthritis. This role will focus on ensuring readiness for large,...

Contract Length: 12 monthsWorkload: 20 hours/weekLocation: UK-based roleStart Date: February Engagement: B2BRole Overview:We are seeking an experienced CMC leader to drive Chemistry, Manufacturing & Controls (CMC) activities for the late-stage clinical development of a novel Fc-fusion protein targeting NT-3 for chronic pain and osteoarthritis. This role will focus on ensuring readiness for large,...