Analytical Method Validation Lead – GMP QC (On-site)

Eurofins; Waver; Sur place; EUR 55 000 - 75 000; Plein temps

Avantages offerts par ce poste

Meal vouchers 8 Euro/Working Day

Eco-Cheques 250 Euro/Year

DKV Hospitalization insurance

12 ADV days

Well-being program

Payflip app

Résumé du poste

Eurofins PSS Insourcing Solutions is hiring an Analytical Method Validation Specialist to support QC Operations in a GMP pharmaceutical environment. The role involves coordinating validation studies, authoring validation documentation, and ensuring compliance with quality systems.

You will work with laboratories, statisticians, and quality representatives to drive critical validation projects, with a focus on continuous improvement and method lifecycle management.

Qualifications

• Master’s degree in a relevant scientific discipline.
• 3–5 years of pharma QC/analytical development/validation experience.
• Strong analytical method validation experience in a GMP environment.
• Experience authoring technical and validation documentation.
• Experience with Change Control, Deviation Management and CAPA.

Responsabilités

• Author and maintain validation documentation: protocols, reports, amendments, risk assessments, rationales, instructions, reviews.
• Coordinate validation activities across multiple stakeholders and teams.
• Support quality events linked to validation: deviations, CCs, CAPAs; participate in investigations.
• Participate in peer and quality reviews to maintain validated methods.
• Identify opportunities to improve validation processes and documentation quality.

Connaissances

Fluent English

French (nice to have)

Formation

Master’s degree in Chemistry/Biochemistry/Pharmaceutical Sciences

Description du poste

Eurofins PSS Insourcing Solutions is hiring an Analytical Method Validation Specialist to support QC Operations in a GMP pharmaceutical environment. The role involves coordinating validation studies, authoring validation documentation, and ensuring compliance with quality systems.

You will work with laboratories, statisticians, and quality representatives to drive critical validation projects, with a focus on continuous improvement and method lifecycle management.