Analytical Method Validation Specialist

Eurofins · Wallonia, Belgium

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Role summary

Eurofins seeks an Analytical Method Validation Specialist to coordinate and document validation activities in a pharmaceutical manufacturing setting. The role involves authoring validation protocols, managing cross-functional projects, and ensuring GMP compliance while supporting quality initiatives.

What they're looking for

Master's degree in chemistry, biochemistry, pharmaceutical sciences, biotechnology, or related field
Minimum 1.5 years pharmaceutical quality control, analytical development, validation, or QA experience
Strong experience with analytical method validation in GMP-regulated environments
Experience authoring technical and validation documentation
Experience managing change controls, deviations, and CAPA processes
Fluent English communication skills; French proficiency preferred

What you'll be doing

Author and maintain validation documentation including protocols, reports, risk assessments, and technical instructions
Coordinate validation activities across laboratories, project teams, quality representatives, and statisticians
Monitor validation studies, manage data collection, analyze results, and ensure proper documentation
Support quality events including deviations, change controls, and CAPA investigations
Participate in peer review, compliance activities, and continuous improvement projects within QC operations

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