Analytical Method Validation Specialist – QC, Flexible Hours

Eurofins; Sint-Katelijne-Waver; Sur place; EUR 65 000 - 85 000; Plein temps

Avantages offerts par ce poste

Eco-Cheques

ADV days

Team lunches

Well-being program

Payflip access

Résumé du poste

Eurofins PSS Insourcing Solutions® in Belgium seeks an experienced Analytical Method Validation Specialist to support QC operations in a GMP-regulated pharmaceutical environment.

The role coordinates validation activities, authors validation documentation, and collaborates with laboratories, statisticians, and QA. Full-time on-site in Wavre with strong emphasis on continuous improvement and quality excellence.

Qualifications

• Master’s degree in chemistry or related field with GMP exposure.
• 3-5 years of pharma QC/Analytical Development, Validation, or QA experience.
• Experience authoring technical and validation documentation and handling CAPA/Change control.

Responsabilités

• Author and maintain validation documentation: protocols, reports, amendments, risk assessments, and scientific rationales.
• Coordinate validation activities across multiple stakeholders and teams.
• Support quality systems: deviations, CC, CAPA, investigations and meetings.
• Assist in risk-based decisions for method lifecycle management and continuous improvement.

Connaissances

English (Fluent)

French (Nice to have)

Formation

Master’s degree in chemistry

Description du poste

Eurofins PSS Insourcing Solutions® in Belgium seeks an experienced Analytical Method Validation Specialist to support QC operations in a GMP-regulated pharmaceutical environment.

The role coordinates validation activities, authors validation documentation, and collaborates with laboratories, statisticians, and QA. Full-time on-site in Wavre with strong emphasis on continuous improvement and quality excellence.