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Senior Validation Engineer
Negotiable

Senior Validation Engineer (Contract)Location: Hertfordshire (Hybrid/On-site as required) Contract: 6+ Months Industry: Medical Devices / Life Sciences We're supporting a medical device manufacturer through a significant operational expansion and product transfer project within one of its key UK sites.As part of a large scale investment in manufact...

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...

QA Specialist Serialization and Automation (12 months)
BrusselsNegotiable

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 ...

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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...

Quality Engineer
PrahaNegotiable

Medical Device Quality Engineer - 6 months Location: Prague, Czech RepublicContract Length: 6 Months (Potential Extension)Start Date: ASAPWorking Pattern: 3 Days Onsite / 2 Days Remote Company Overview Our client is a leading global medical device organisation seeking an experienced Quality Engineer to support critical Quality Management System (Q...

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...