Senior QC Specialist (GLP Studies – Product Safety Labs)

SmartRecruiters, Inc.; Bengaluru; On-site; INR 1,800,000 - 2,400,000; Full time

Job summary

Eurofins Scientific is seeking a Senior QC Specialist for GLP studies in Product Safety Labs in Bengaluru. The role focuses on advanced QC reviews of study data and documentation to ensure accuracy, completeness, and inspection readiness.

Ideal candidates hold a Bachelor’s in a related field with 8–12 years in GLP environments, and a Master’s degree is preferred. The position is full-time with opportunities to lead quality initiatives and process improvements.

Qualifications

• Bachelor’s degree in Toxicology, Biology, Pharmacology, Pharmaceutical Sciences, or related field is required or preferred with strong GLP knowledge.
• 8–12 years of experience in GLP-regulated environments, CRO operations, preclinical research, QA/QC, or study support.

Responsibilities

• Perform detailed QC reviews of laboratory data, worksheets, protocols, amendments, and study records.
• Conduct first-pass review of complex and long‑term study datasets.
• Identify documentation discrepancies, omissions, transcription errors, and data inconsistencies.
• Coordinate correction and resolution of quality issues and verify completion.
• Maintain audit‑ready study files and records.
• Support preparation of study data packages for reporting, archival, and inspection readiness.

Education

Bachelor’s degree in Toxicology, Biology, Pharmacology, Pharmaceutical Sciences, or related field

Master’s degree (preferred)

Job description

Senior QC Specialist (GLP Studies – Product Safety Labs)

Full-time

ENGLISH

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 2020, Eurofins generated 5.4 billion Euro proforma turnover in 800 laboratories across 50 countries, employing about 50.000 staff.

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.

Essential Duties and Responsibilities:

• Perform detailed QC reviews of laboratory data (acute toxicology data), worksheets, protocols, amendments, and study records.
• Conduct first-pass review of complex and long‑term study datasets.
• Identify documentation discrepancies, omissions, transcription errors, and data inconsistencies.
• Coordinate correction and resolution of quality issues and verify completion.
• Review study trackers, shipping records, chain-of-custody documents, and supporting study documentation.
• Maintain 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.
• Develop 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.

Basic Minimum Qualifications (BMQ):

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; Master’s preferred.
• 8–12 years of experience in GLP-regulated environments, CRO operations, preclinical research, QA/QC, or study support.
• Strong knowledge of GLP regulations, data integrity principles, and good documentation practices.

All candidate CV's and cover letter's will be reviewed, however please note that we are not always able to respond to every expression of interest submitted. Â