Global Validation/Verification coordinator

Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing.

In 2018, Eurofins generated 4.2 billion Euro proforma turnover in 800 laboratories across 47 countries, employing about 45.000 staff.

The Validation/Verification Coordinator coordinates the implementation of (new or updated) laboratory tests in compliance with applicable regulatory requirements and quality standards. Coordinates and oversees test validation and verification activities, associated documentation, and QA and CAP Director reviews to ensure timely report approval and support successful test implementation.

Key Accountabilities

Coordinate global validation or verification of laboratory tests.

Align with operational teams and laboratories on required activities and documentation.

Define and track validation/verification milestones with relevant stakeholders.

Ensure compliance with global validation and verification standards.

Complete, review, and approve all documentation, including final signed validation/verification reports.

Master's degree in Biochemistry/Life Sciences, or a bachelor’s degree with relevant experience.

Minimum of 5-10 years of (medical) clinical laboratory experience, including at least 1-2 years of experience writing clinical laboratory validation/verification reports.

Prior hands-on experience in method verification/validation is required.

Working knowledge of EP Evaluator or similar statistical software for clinical laboratory validation/verification is required; familiarity with EP Evaluator specifically is preferred.

Abilities and/or Skills:

Honest, Dependable, Demonstrated Ability to Self-Manage

Detail Oriented, Accurate, Precise

Strong Math Skills

Strong Organizational Skills

Logical Thinking, Good Reasoning Ability

Strong communication including verbal, writing, and presentation skills

Dedication to quality, ethics, and customer service

Ability to handle personal stress

Mental and emotional stability and maturity

Motivation to excel

Should be able to sit for long periods as per role requirement

Team Lead experience