Eurofins: Study Support 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 Study Support Specialist (GLP studies – Product Safety Labs) in Bengaluru, KA, India, under reference REF81679Z. 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: 30 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:
• To better support the Study Director function and allow them to focus on scientific oversight and regulatory accountability
• Collaboration: with lab staff to gather study requirements, test article information, and study design details necessary for study initiation, laboratory assignment, and resource planning
• Research / execution: quality control reviews of laboratory data, worksheets, and study records to ensure accuracy, completeness, consistency, and readiness for Study Director review which will include long-term and complex studies generating extensive datasets
• Monitoring: study milestones, deliverables, and critical path activities to proactively identify risks, communicate potential delays, and support on-time completion of client commitments and regulatory deadlines
• Coordination: the development, review, revision, and issuance of study protocols, amendments, and associated study documentation in accordance with GLP requirements and internal procedures
• Maintenance: study documentation and tracking systems, ensuring study files remain audit-ready and compliant with applicable quality standards throughout the study lifecycle
• Support: the preparation of shipping documentation and return authorizations for test articles, samples, and retained materials, while obtaining, reviewing, and maintaining chain-of-custody records and shipment tracking information
• Support: Study Directors with scheduling, study logistics, sample management, and cross-functional communication among laboratory, quality assurance, and/or project management
• Tracking: study-related actions, deviations, data requests, and documentation to ensure timely resolution and complete study records
• Support: the compilation, review, and organization of study data packages for report generation, archival, and regulatory inspection readiness
• Delivery: technical writing support for projects which may include generating shell documents and tables of data that was collected over the course of a study
• Trend study control performance and study outcome
• Review: study data to ensure activities were executed according to protocol requirements, SOP, approved timelines, and GLP expectations

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):
• Master’s degree in a science-related (Pharmacology / Toxicology would be a best fit) field with 5-7 years of experience in Pre-clinical studies / trials, IND enabling studies, IND filing and with knowledge of regulatory requirements (GLP)

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 Study Support Specialist (GLP studies – Product Safety Labs) vacancy is not an offer for reference REF81679Z; 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 REF81679Z.

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
• quality assurance
• GLP
• laboratory testing
• audit
• project management
• logistics
• communication
• pharmacy