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 1.5 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

• Full-time (40 hours/week) Monday – Friday job
• 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