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

Application Link