Contract Manufacturing Jobs
Showing 42 results
Sort by:
External Quality Senior Specialist
Our client is seeking an experienced External Quality Senior Specialist to support Quality Process & Operations activities within a global pharmaceutical environment. This role focuses on strengthening External Quality processes, supplier oversight, quality systems management, regulatory compliance, and continuous improvement initiatives across ex...
Asset CQV Engineer
Asset Engineer (CQV) - Ghent, Belgium (Fully Onsite)OverviewWe are seeking an experienced Asset Engineer (Commissioning, Qualification & Validation) to join a leading pharmaceutical manufacturing facility in Ghent, Belgium. This position is responsible for ensuring manufacturing equipment, utilities, and systems remain qualified, compliant, and in ...
Senior Process Engineer Sterile Polymer (Contract)
OverviewWe are seeking an experienced pharmaceutical engineering professional to lead the development and implementation of a novel aseptic manufacturing process for biodegradable polymer-based implant products.This role will take ownership of process design, equipment integration, supplier coordination, installation activities, and qualification s...
Elevate your career
Take the first step toward your next opportunity - submit your CV and get started today.
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 ...
Senior CQV Engineer
Role Overview We are looking for a Senior CQV Engineer for a duration of 12 months, to support pharmaceutical manufacturing projects, with primary responsibility for commissioning and qualification of GMP manufacturing equipment. The role requires a hands-on engineering profile capable of independently driving CQV activities from planning and proto...
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...