QA, Qualification & Validation Systems Lead

PIERRE FABRE MEDICAMENT; Gaillac; On-site; EUR 60,000 - 90,000; Full time

Job summary

Pierre Fabre Laboratories in France seeks a senior QA/Validation Lead to define and govern validation plans for equipment, processes and IT systems across our production sites. You will approve master plans, drive qualification activities and ensure systems remain qualified.

Bring 5+ years of QA/validation experience in the pharmaceutical industry, strong leadership, and the ability to implement compliant validation strategies that support product quality and patient safety.

Qualifications

• 5+ years of QA/validation experience in pharma production.
• Experience with qualification/validation and CSV.
• Proven leadership and people management skills.

Responsibilities

• Define validation master plans for equipment, processes and IT systems.
• Steer qualification/validation to keep systems in valid state.
• Schedule qualifications/validation activities and oversee execution.
• Lead and develop the QA/validation team.

Skills

AQ experience

Qualification/validation experience

Team management

GMP knowledge

Education

Master's degree in pharmaceutical sciences or related field

Job description

Pierre Fabre Laboratories in France seeks a senior QA/Validation Lead to define and govern validation plans for equipment, processes and IT systems across our production sites. You will approve master plans, drive qualification activities and ensure systems remain qualified.

Bring 5+ years of QA/validation experience in the pharmaceutical industry, strong leadership, and the ability to implement compliant validation strategies that support product quality and patient safety.