CSV Engineer

• Lead validation activities for computerized equipment and control systems, including generating and executing validation documentation (DQ, IQ, OQ, PQ).
• Manage validation projects ensuring compliance with Sanofi policies, cGMP, and regulatory requirements (US FDA, EU).
• Participate in change control processes and approve validation/revalidation plans and site change controls.
• Provide technical support related to lyophilization, aseptic processing, sterilization, and other critical manufacturing systems.
• Maintain validation documentation and ensure continuous compliance with quality management systems and KPIs.

• Degree in Science (preferably Chemistry, Microbiology, Pharmacy) or Engineering (Chemical, Mechanical, Electrical), with post-graduate qualifications a plus.
• 3-5 years' experience in healthcare manufacturing, ideally pharmaceutical, with 2-3 years in a validation role.
• Strong knowledge of GAMP, ISPE Baseline guides, quality and compliance regulations, and pharmaceutical plant operations.
• Skilled in troubleshooting validation issues, project management, and effective communication across teams.
• Personal traits include being motivated, adaptable, pragmatic, a natural influencer, and able to see projects through completion.

Cpl Group