YOUR NEXT OPPORTUNITY
Global Validation/Verification coordinator
Eurofins
Employer posted: September 28, 2026. Source checked: October 6, 2026 1:51 pm. Availability and final application requirements are confirmed on the employer’s site.
Source: Eurofins — India. WorkerEra lists this opportunity from an external source; confirm current details with the employer.
About this opportunity
Company Description
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.
Job Description
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.
Qualifications
Education
- Master’s degree in Biochemistry/Life Sciences, or a bachelor’s degree with relevant experience.
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.
Additional Information
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
Your application checklist
- Read the linked employer announcement and compare its requirements with your experience.
- Tailor your CV to responsibilities and skills actually listed by the employer.
- Confirm the work location, deadline and application documents before submitting.
- Salary was not supplied in the listing fields; ask the employer about compensation.
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