Contract Quality Jobs
Showing 22 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...
Sterility Assurance Consultant (6 months+)
We are supporting a client in the Netherlands who is seeking an experienced Sterility Assurance and Contamination Control Consultant for an initial 6+ month engagement. This is a site-based position requiring regular presence on-site, supporting critical quality and microbiological activities within a regulated manufacturing environment.The success...
IT Validation Specialist (12 months)
We are seeking an experienced IT Validation Specialist to support validation and compliance activities for GxP-regulated systems within a highly regulated life sciences environment. The position will play a critical role in ensuring that IT and automation solutions are implemented using risk-based validation methodologies while maintaining complian...
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 ...
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...
Interim QA Director
OverviewAn established pharmaceutical organisation is seeking an experienced Interim QA Director to support a critical sterile manufacturing operation in Tampa, Florida. This is a high-priority 12-month contract requiring an accomplished quality leader with a substantial track record leading Quality Assurance functions within regulated sterile fill...
