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Supplier Quality Engineer
SligoNegotiable

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...

QC Microbiology Specialist
Negotiable

QC Microbiology Specialist (Contract)6-12 Month Contract | Food & Beverage IndustryWe are seeking an experienced QC Microbiology Specialist to support quality operations within a leading food and beverage manufacturing environment. This is a hands-on contract role focused on microbiological testing, environmental monitoring, quality investigations,...

QA-CSV Specialist & Site Key User
BeerseNegotiable

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
VeronaNegotiable

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
KasterleeNegotiable

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
BranchburgNegotiable

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 ...