Contract Manufacturing Engineer Jobs
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Senior Process Engineer (6 months)
Senior Process EngineerLocation: Clermont-Ferrand, France Contract: Freelance Contractor Duration: 6 Months Language: French Preferred OverviewWe are seeking an experienced Senior Process Engineer to support a key manufacturing project near Clermont-Ferrand. The successful candidate will play a critical role in ensuring equipment, systems, document...
CQV Consultant
CQV Consultant (Contract)Location: Lyon Region, France (On-site) Contract Length: 12 Months Industry: Pharmaceuticals Start Date: ASAPThe OpportunityWe are supporting a leading pharmaceutical manufacturing site undergoing a significant capital investment and expansion programme. As part of this project, we are seeking an experienced CQV Consultant ...
Process Engineer
Key ResponsibilitiesSupport and execute process and technology transfer activities for sterile drug products.Prepare, review, and author GMP-compliant technical documentation and transfer packages.Evaluate manufacturing processes, equipment suitability, process performance data, and facility readiness.Review deviations, investigations, CAPAs, proce...
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Asset CQV Engineer
Asset Engineer (CQV) - Ghent, Belgium (Fully Onsite)OverviewWe are seeking an experienced Asset Engineer (Commissioning, Qualification & Validation) to join a leading pharmaceutical manufacturing facility in Ghent, Belgium. This position is responsible for ensuring manufacturing equipment, utilities, and systems remain qualified, compliant, and in ...
Senior Process Engineer Sterile Polymer (Contract)
OverviewWe are seeking an experienced pharmaceutical engineering professional to lead the development and implementation of a novel aseptic manufacturing process for biodegradable polymer-based implant products.This role will take ownership of process design, equipment integration, supplier coordination, installation activities, and qualification s...
Senior CQV Engineer
Role Overview We are looking for a Senior CQV Engineer for a duration of 12 months, to support pharmaceutical manufacturing projects, with primary responsibility for commissioning and qualification of GMP manufacturing equipment. The role requires a hands-on engineering profile capable of independently driving CQV activities from planning and proto...