On Site Contract Quality Jobs

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...

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...

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 ...

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...

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 ...