Analytical Method Validation Specialist

📋 Description

• Author and maintain validation-related documentation including validation protocols, validation
• Coordinate validation activities across multiple stakeholders.
• Collaborate with laboratories, project teams, quality representatives, and statisticians.
• Monitor validation studies and experimental progress.
• Coordinate pre-tests, validation studies, data collection, and reporting activities.
• Analyze validation results and ensure appropriate documentation of outcomes.

🎯 Requirements

• Master’s degree in chemistry, Biochemistry, Pharmaceutical Sciences, Biotechnology, or related
• Minimum 3-5 years of experience in pharmaceutical Quality Control, Analytical Development
• Strong experience with analytical method validation in a GMP-regulated environment.
• Experience authoring technical and validation documentation.
• Experience with Change control, Deviation Management and CAPA management.
• Fluent communication skills in English. French is a plus.

🎁 Benefits

• A full-time (40hours/week) Monday – Friday job.
• A Permanent contract with flexible working hours. (Can start between 7am and 9:30am)
• Place of work: Wavre, Belgium.
• Meal Vouchers 8 Euro/Working Day.
• Eco-Cheques +/- 250 Euro/Year.
• DKV Hospitalization insurance.