Analytical Method Validation Specialist

📋 Description

• Author and maintain validation-related documentation including validation protocols, reports
• Coordinate validation activities across multiple stakeholders, collaborating with laboratories
• Monitor validation studies and experimental progress, coordinate pre-tests, validation studies
• Analyze validation results and ensure appropriate documentation of outcomes.
• Support and coordinate quality events linked to validation activities, including deviations, change
• Participate in investigations and associated meetings, ensuring compliance with internal quality

🎯 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 both French and English.

🎁 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 of 8 Euro per working day.
• Eco-cheques of +/- 250 Euro per year.
• DKV Hospitalization insurance.