CSV Validation Lead - Life Sciences

Evotec; Toulouse; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading biotech company in Toulouse is looking for a CSV Manager to oversee validation projects and lead teams. You will be responsible for ensuring compliance with EU GMP and FDA standards while managing cross-functional activities. The ideal candidate has extensive experience in validation within the pharmaceutical industry and possesses strong leadership skills. Join us for exciting growth opportunities and a flexible work environment.

Prestations

Growth Opportunities

Flexible Work Environment

Inclusive Culture

Innovative Projects

A Place for Big Ideas

Qualifications

• 12+ years in validation/qualification in pharma or biotech, including 4+ years in a managerial role.
• Strong knowledge of regulatory standards: EU GMP, FDA CFR.
• Proven expertise in computerized systems validation (CSV).
• Solid track record in audit management.

Responsabilités

• Manage a team of validation engineers and oversee external contractors.
• Develop and maintain the Validation Master Plan (VMP).
• Lead validation lifecycle programs for computerized systems (CSV).
• Ensure compliance with quality standards.

Connaissances

Leadership

Strong communication

Analytical mindset

Project management

Formation

Master’s degree in Engineering, Pharmacy, Life Sciences, or equivalent

Description du poste

A leading biotech company in Toulouse is looking for a CSV Manager to oversee validation projects and lead teams. You will be responsible for ensuring compliance with EU GMP and FDA standards while managing cross-functional activities. The ideal candidate has extensive experience in validation within the pharmaceutical industry and possesses strong leadership skills. Join us for exciting growth opportunities and a flexible work environment.