Contract Compliance Jobs
Showing 19 results
Sort by:
Regulatory Affairs & Quality Consultant
Location: Lyon, France (Hybrid) Contract Length: 12 Months Start Date: Mid-October 2026 Engagement: Freelance We're supporting an established medical technology organisation developing innovative drug delivery and combination products. They are seeking an experienced Regulatory Affairs & Quality Consultant to lead key regulatory and quality initia...
Plasma Fractionation Specialist
OverviewWe are seeking an experienced pharmaceutical professional with direct plasma fractionation manufacturing experience to support ongoing operations and project activities at a pharmaceutical site in Strasbourg.The role is open to candidates from a range of backgrounds, including Process Engineering, CQV, Manufacturing, Production, Validation...
QMS Consultant
OverviewWe are seeking an experienced Quality Systems Manager to lead and continuously improve the Quality Management System (QMS) within a GMP-regulated pharmaceutical environment. This role will be responsible for ensuring compliance with global regulatory requirements while driving quality excellence across manufacturing, laboratory, supply chai...
Elevate your career
Take the first step toward your next opportunity - submit your CV and get started today.
Supplier Quality Engineer
Supplier Quality Engineer | 12 Month Contract Location: North of Ireland (Must be based in Ireland) Onsite Requirement: 5 days per week Contract Length: 12 Months A leading healthcare manufacturer is seeking a Supplier Quality Engineer to support quality oversight activities across its third-party manufacturing network. This role will act as the ke...
QA Specialist Serialization and Automation (12 months)
OverviewWe are seeking an experienced Quality Assurance professional to represent Global Quality on two strategic cross-functional programmes within a pharmaceutical manufacturing environment.The primary focus of the role is a global serialization transformation initiative, where the successful candidate will lead the development and deployment of ...
QA-CSV Specialist & Site Key User
QA-CSV Specialist & Checklyst Manager Site Key UserLocation: Belgium (On-Site) Contract End Date: 31 December 2026 / 2027 ( there is one role ending 2026 and one ending 2027) Function: Quality / Validation Industry: Pharmaceutical ManufacturingAbout the RoleWe are seeking a QA-CSV Specialist & Checklyst Manager Site Key User to support a leading p...