Eurofins: Global Validation/Verification coordinator — Bengaluru, KA, India

About Eurofins

Eurofins provides analytical testing and laboratory services across life sciences and other industries. Its work includes assessing food, water, pharmaceutical and cosmetic products for qualities such as safety, authenticity, composition and accurate labelling. The employer also describes activities in genomics, clinical-study support, biopharmaceutical development and manufacturing, and diagnostic testing. Scientific methods and dependable information are central to this business, supported by the technology and operational functions used to deliver laboratory services.

The position and its setting

Eurofins lists Global Validation/Verification coordinator in Bengaluru, KA, India, under reference REF81665T. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

• Department: Testing & Laboratory
• Employment type: Full-time
• Employer listing date: 15 October 2026
• Legal Entity: CIN003 - Eurofins Pharma Services India Pvt Ltd.
• Contract Type: Temporary / Fixed Term
• Business Lines: Other Business Line
• Brands: Eurofins

Responsibilities and work described

• 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
• Coordination: 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
• Quality / delivery: compliance with global validation and verification standards
• Complete, review, and approve all documentation, including final signed validation/verification reports

Essential requirements and candidate background

• Education
• 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
• Exeperience in hematology, clinical chemistry and serology, flow cytrometry and molecular biology
• Prior hands-on experience in method verification/validation is required

Preferred experience and additional strengths

• Knowledge: EP Evaluator or similar statistical software for clinical laboratory validation/verification is required; familiarity with EP Evaluator specifically is preferred

Location, schedule and contract conditions

• Work arrangement: On-site
• Advertised location: Bengaluru, KA, India

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Global Validation/Verification coordinator vacancy is not an offer for reference REF81665T; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Eurofins

Applications follow the official employer page linked below.

Open the official Eurofins posting below and match the title and reference REF81665T.

Compare your qualifications and experience with the essential conditions for the Bengaluru, KA, India position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: laboratory testing

Laboratory experience is clearer when it names the sample or test context, the method and the checks used to establish a valid result. Explain record keeping, review and your own responsibility.

Relevant skills

• laboratory testing
• compliance
• stakeholder management
• key-account planning
• chemistry