On Site Contract Quality Jobs
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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...
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...
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AVI Engineer
Contract Opportunity | Pharmaceutical Manufacturing | Visual InspectionWe are supporting a pharmaceutical manufacturer seeking an experienced AVI Engineer with strong hands-on expertise in Koerber visual inspection systems for vials.This is a specialist assignment focused on the development, optimisation, and qualification of inspection recipes on ...
Process Engineer Visual Inspection
We are seeking an experienced Process Engineer VI to support critical Visual Inspection (VI) and Container Closure Integrity Testing (CCIT) initiatives within a GMP-regulated pharmaceutical manufacturing environment. This position will play a key role in the implementation, qualification, optimization, and lifecycle management of advanced inspectio...
Validation Specialist
We are seeking an experienced Validation Specialist to support validation activities within a state-of-the-art aseptic manufacturing facility. This role will focus on ensuring GMP compliance across critical manufacturing systems, equipment, facilities, and processes involved in sterile drug product manufacturing.The successful candidate will work ...
