QA Validation

QA Validation Officer

Brabant Wallon Contracting

Your Responsibilities:

• Review and approval of validation documentation (URS, protocols, reports) in compliance with GMP standards
• Supervision and quality oversight of validation activities (IQ, OQ, PQ)
• Ensure proper execution and documentation of FAT (Factory Acceptance Testing) and SAT (Site Acceptance Testing)
• Support equipment qualification processes from installation through performance qualification
• Collaborate with internal and external stakeholders to ensure validation strategy alignment
• Ensure compliance with company procedures and regulatory expectations (FDA, EMA)
• Provide QA input during audits and inspections as a subject matter expert on validation

Your Profile:

• Proven experience in a GMP-regulated environment, ideally at GSK or similar
• Solid background in equipment validation (IQ, OQ, PQ)
• Knowledge of validation methodologies, including FAT and SAT
• Familiarity with pharmaceutical manufacturing and quality systems
• Fluent in English and French (spoken and written)
• Strong attention to detail, organizational skills, and a proactive mindset
• Ability to work cross-functionally and communicate effectively with technical and QA teams

Our Offer:

Jefferson Wells offers you a permanent consultant contract with a competitive salary and a wide range of training opportunities. As your trusted career partner, we'll support you every step of the way.

Interested? Send your CV to