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External Quality Senior Specialist
Beerse€50 - €70 EUR a day

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...

Data Integrity Lead
LyonNegotiable

Data Integrity & CSV Program ManagerLocation: Lyon, France Start: Approximately 1-2 months Duration: 12 months Language: Fluent French requiredRole OverviewWe are seeking an experienced Data Integrity & CSV Program Manager to lead a large-scale Data Integrity programme within a pharmaceutical manufacturing environment.The programme will involve the...

Plasma Fractionation Specialist
StrasbourgNegotiable

OverviewWe are seeking an experienced pharmaceutical professional with direct plasma fractionation manufacturing experience to support ongoing operations and project activities at a pharmaceutical site in Strasbourg.The role is open to candidates from a range of backgrounds, including Process Engineering, CQV, Manufacturing, Production, Validation...

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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 ...

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...

Interim QA Director
TampaNegotiable

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...