Eurofins: Senior QC Specialist (GLP Studies – Product Safety Labs) — 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 Senior QC Specialist (GLP Studies – Product Safety Labs) in Bengaluru, KA, India, under reference REF81675T. 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: 28 September 2026
• Legal Entity: CIN003 - Eurofins Pharma Services India Pvt Ltd.
• Contract Type: Permanent
• Business Lines: Other Business Line
• Brands: Eurofins

Responsibilities and work described

• Position Summary:
• The Senior QC Specialist performs advanced quality control reviews of study data, documentation, and records supporting GLP-compliant preclinical studies
• The role ensures study records are accurate, complete, consistent, and inspection-ready before Study Director review while supporting continuous improvement and data integrity initiatives
• Execution: detailed QC reviews of laboratory data ( acute toxicology data ), worksheets, protocols, amendments, and study records
• Research / execution: first-pass review of complex and long-term study datasets
• Identify documentation discrepancies, omissions, transcription errors, and data inconsistencies
• Coordination: correction and resolution of quality issues and verify completion
• Review: study trackers, shipping records, chain-of-custody documents, and supporting study documentation
• Maintenance: audit-ready study files and records
• Support: preparation of study data packages for reporting, archival, and inspection readiness
• Trend recurring quality issues and recommend corrective and preventive actions
• Development: and maintain QC checklists and review standards
• Mentor support staff regarding documentation quality expectations
• Participate in process improvement initiatives
• Escalate significant scientific, regulatory, or quality issues appropriately

Essential requirements and candidate background

• To perform this job successfully, the individual must be able to perform each essential duty satisfactorily
• The requirements below are representative of the knowledge, skill or ability required
• Education/Experience (BMQ):
• Bachelor’s degree in Toxicology, Biology, Pharmacology, Pharmaceutical Sciences, or related field
• 8–12 years of experience in GLP-regulated environments, CRO operations, preclinical research, QA/QC, or study support
• Knowledge: GLP regulations, data integrity principles, and good documentation practices

Education and qualification routes

• Degree / qualification: Master’s 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 Senior QC Specialist (GLP Studies – Product Safety Labs) vacancy is not an offer for reference REF81675T; 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 REF81675T.

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: quality control

Quality-control experience is clearer when it describes what was checked, the acceptance basis and how a non-conforming result was handled. Include the records or review process where those were part of your work.

Relevant skills

• quality control
• process improvement
• GLP
• laboratory testing
• audit
• clinical research
• pharmacy