pharmacovigilance cqc specialist

The Pharmacovigilance (PV) Case Quality Check (CQC) Specialist plays a critical role in ensuring the accuracy, completeness, and compliance of pharmacovigilance cases.

This position involves meticulous review and validation of safety data and documentation to guarantee adherence to regulatory requirements and internal standards. The specialist will collaborate with cross-functional teams to identify and rectify discrepancies, contributing to the overall quality of pharmacovigilance processes. 

• Bachelor/master degree in life sciences, animal health, veterinary medical technology, veterinary medicine, nursing, pharmacy, biochemistry, zoology or a related discipline. 
• 3 to 5 years of experience in the pharmaceutical/biotechnology area and/or quality-related area.
• Experience in the pharmaceutical industry within the regulated area of pharmacovigilance.
• Experience with case data entry in applicable PV database and/or case quality requirements is preferred.
• Experience in AI, machine learning and/or advanced MS Office would be an asset.
• Experience working in an international, multicultural, and transversal environment.
• Familiarity with GxP systems in the pharmaceutical industry, including knowledge of applicable regulations, computerized system validation, GXP principles, and practices.
• Familiarity with statistical, quality, and data integrity principles.
• Fluent in English & good knowledge of French.

We offer an attractive salary with benefits (car, insurance, monthly allowance, 7 euros meal voucher per day, ...). A rate as freelancer is also possible.