Contract Quality Engineer Jobs
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Continued Process Verification Consultant
Location: Anagni, ScoppitoContract length: 9-10 monthsNumber of positions: 6OverviewWe are supporting the implementation of a global Continued Process Verification (CPV) programme across pharmaceutical manufacturing sites in Italy. Consultants will play a key role in establishing site-level CPV strategies aligned with standardised global guidance ...
Software Quality engineer
Software Validation & Quality SpecialistResponsible for ensuring all equipment and software qualification activities are completed in compliance with global/site procedures, regulatory requirements, and quality standards. This includes providing guidance across the full software lifecycle, covering equipment with software, standalone software syste...
GMP Qualification & Validation Consultants
Location: Toulouse Area, France Contract: Freelance / Consulting Assignment Industry: Pharmaceutical Manufacturing / CDMO Start: Q3/Q4 2026The ProjectWe are supporting a major pharmaceutical manufacturing site in the Toulouse area that is undergoing significant expansion and operational growth.Multiple projects are running simultaneously across m...
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Qualification & Validation Responsible
Location: Brussels, Belgium Start date: ASAPOverviewWe are seeking an experienced Qualification, Validation & Metrology Manager to support GMP-regulated pharmaceutical manufacturing operations. The successful candidate will lead qualification and validation activities, oversee metrology programmes, and ensure compliance with regulatory and quality ...
Quality Engineer Metrology
Metrology Quality Engineer (12-Month Contract)📍 France | 🏥 Medical Device ManufacturingWe are supporting a leading medical device manufacturer in their search for an experienced Metrology Quality Engineer to join their site on an initial 12-month contract.This is a high-impact role focused on establishing and developing an on-site Metrology and ...
Quality Specialist
Contract DetailsStart Date: ImmediatelyLocation: Montpellier, France (5 days on-site)Hours: 40 hours per week (full-time)Engagement: 6 month Freelance Contract Key ResponsibilitiesEnsure the Quality Management System remains compliant with internal procedures and applicable global regulatory requirements, including ISO 13485, EU MDR, FDA QSR/QMSR, ...