Data Reviewer, Chemistry – Raw Materials (Full-Time)
Bengaluru, Karnataka, India
Company Overview
Eurofins Scientific is a leading global life sciences organization providing a comprehensive range of analytical testing services across pharmaceutical, food, environmental, and cosmetic industries. The company supports product safety, authenticity, and regulatory compliance through advanced laboratory testing, clinical study support, genomics services, and specialized diagnostic solutions. With a strong global presence and an extensive laboratory network, Eurofins plays a critical role in advancing quality and innovation across the healthcare and pharmaceutical sectors.
Job Overview
The Data Reviewer, Chemistry – Raw Materials is responsible for ensuring the accuracy, quality, and regulatory compliance of laboratory data related to pharmaceutical raw materials testing. The role focuses on reviewing analytical data, validating documentation, and ensuring adherence to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
This position requires strong technical knowledge of analytical chemistry processes, attention to detail, and the ability to maintain high-quality standards within regulated pharmaceutical environments.
Key Responsibilities
Review laboratory data to ensure accuracy, completeness, and compliance with GMP and GLP requirements.
Evaluate analytical documentation, calculated results, and final reports according to departmental, corporate, and client Standard Operating Procedures (SOPs).
Interpret and understand analytical testing procedures and methodologies.
Develop technical knowledge of analytical techniques used in pharmaceutical raw material testing.
Ensure data integrity and clarity in all laboratory records and reporting.
Apply regulatory compliance standards across all areas of responsibility.
Utilize MS Office applications including Excel, Word, Access, and Outlook for data review and reporting.
Conduct activities in accordance with safety and quality standards.
Support continuous improvement initiatives and perform additional duties as assigned.
Education and Experience Requirements
Master’s degree in Pharmaceutical Chemistry, Analytical Chemistry, or a related discipline.
0–2 years of experience in analytical testing of pharmaceutical raw materials preferred.
Exposure to raw material testing parameters such as ROI, LOD, pH, Karl Fischer (KF), or related analytical methods is desirable.
Experience working in GMP-regulated environments is an advantage.
Required Skills and Competencies
Strong attention to detail and commitment to data accuracy and quality assurance.
Excellent analytical thinking and problem-solving abilities.
Effective verbal and written communication skills.
Ability to manage multiple tasks and meet deadlines in a regulated environment.
Strong organizational skills and professional judgement.
Proficiency in computer systems and laboratory data management tools.
Logical reasoning and strong numerical aptitude.
Ability to work independently and collaboratively within cross-functional teams.
Career Growth Opportunities
This role provides exposure to pharmaceutical quality control processes, regulatory compliance frameworks, and analytical data review systems. It offers strong career progression opportunities in quality assurance, analytical chemistry, and pharmaceutical laboratory operations.
Job Category: Pharmaceutical Quality Control / Analytical Chemistry / Laboratory Operations
Employment Type: Full-Time
Location: Bengaluru, Karnataka, India
Experience Required: 0–2 years in pharmaceutical analytical testing (preferred)
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