Eurofins Scientific is actively hiring for the role of Data Review – Specialist (Stability Protocol / Study Build Review) in Bengaluru, Karnataka. This opportunity is ideal for candidates with a strong background in pharmaceutical sciences, GMP compliance, and data integrity, looking to build a career in regulated laboratory environments.
Eurofins is a global leader in life sciences testing, offering services in pharmaceuticals, food, environment, and clinical research. With operations in over 60 countries and 950+ laboratories, this role provides exposure to international quality standards and advanced LIMS systems.
🔍 Job Overview
- Role: Data Review Specialist (Stability Protocol / Study Build Review)
- Location: Bengaluru, Karnataka, India
- Company: Eurofins Scientific
- Job Type: Full-time
- Experience: 4–6 years
- Qualification: Master’s in Chemistry, Biology, Pharma, or related field
📌 Key Responsibilities
Training Phase – Protocol Writing & Study Build
- Learn stability protocol writing based on client quotes
- Build stability studies using LIMS systems
- Interpret scientific documentation and client requirements
- Understand end-to-end stability program workflows
Primary Role – Data Review Specialist
- Perform detailed review of stability protocols and study builds
- Verify accuracy of storage conditions, pull points, and test plans
- Ensure compliance with GMP, SOPs, and regulatory standards
- Identify discrepancies and collaborate with internal teams
- Maintain audit-ready documentation aligned with ALCOA+ principles
- Support process improvements in documentation and workflows
🎓 Qualifications & Skills
- Master’s degree in Life Sciences / Pharmaceutical Sciences
- 4–6 years of experience in regulated lab environments
- Strong understanding of GMP and data integrity
- Familiarity with LIMS systems
- Excellent attention to detail and analytical skills
- Strong communication and stakeholder collaboration ability
- Logical reasoning and problem-solving mindset
💼 Salary & Benefits
- Estimated Salary: ₹6,00,000 – ₹10,00,000 per annum
- Exposure to global pharmaceutical projects
- Structured training in protocol writing and study build
- Career growth in CRO and regulatory data management
- Opportunity to work with advanced lab informatics systems
🚀 Why Join Eurofins?
- Global leader in analytical and laboratory services
- Strong presence in pharma, genomics, and clinical research
- Emphasis on quality, compliance, and innovation
- Excellent learning environment for stability studies and GMP
📩 How to Apply
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