Compliance Jobs
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Quality systems manager
We are seeking a Quality Systems Manager to join our team in the South of France on a 12-month contract, with the potential for permanent placement. This is a full-time, on-site role requiring strong French language skills and the ability to operate with autonomy and maturity within a regulated pharmaceutical/biotech environment. Key Responsibiliti...
Senior CSV Specialist
We are seeking a Senior CSV Consultant to lead validation activities across a broad scope of systems. This role sits within the technical operations function, which covers new product introduction, CQV, CSV, automation, and supporting services. The consultant will act as the internal lead for computer system validation, coordinating external consul...
CQV Engineer
This is a contract position with a leading pharmaceutical/biotech organization, requiring candidates to hold full rights to work in France/EU. Successful applicants will support commissioning, qualification, and validation (CQV) activities across multiple French sites. The role offers strong potential for extension and progression into more senior ...
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Quality inspector
Location: Multiple production sites, France (6 sites of interest)Duration: 4-6 months (contract)Start Date: Monday, 22nd December (no work required on 25th December) Shifts:Option A: 12-hour shifts (day/night)Option B: 8-hour shifts (morning/evening/night) Payment Structure:Day shift - standard day rateEvening shift - 1.25x day rateNight shift - ...
Qualification Execution Engineer
About the RoleWe are seeking a Qualification Execution Engineer for a short-term pharmaceutical project. This role involves executing qualification activities for critical manufacturing systems and controlled environments, ensuring compliance with GMP standards.Key ResponsibilitiesParticipate in SAT execution and review SAT reports.Lead full quali...
Regulatory Affairs Consultant (SaMD)
Regulatory Affairs Consultant - Software as a Medical Device (SaMD) Location: France (Remote/Hybrid)Length: 12 monthsStart Date: January 2026 About the RoleWe're looking for an experienced consultant to advise on regulatory and quality strategies for software-driven medical technologies. This role is ideal for someone who understands the complexiti...