Senior Specialist Data Review - Analytical Chemistry

5w1 month ago

Eurofins

Bengaluru, IN · Full-time · INR 1,200,000 – INR 1,700,000

About this role

Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services across multiple industries. The role ensures clients receive quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.

Day-to-day responsibilities include applying GMP/GLP in all areas, reviewing documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs. You will gain a technical understanding of the techniques involved in the review process and use MS Windows applications including Excel, Word, Access, and Outlook.

Eurofins operates 800 laboratories across 47 countries, employing about 45,000 staff. The company is a global leader in food, environment, pharmaceutical, and cosmetics testing, as well as agroscience CRO services, fostering a quality-driven and collaborative environment.

This position offers the opportunity to work with advanced analytical instrumentation and software such as Waters Empower, LIMS, and electronic notebooks. It provides a pathway to deepen expertise in pharmaceutical chemistry data review within a world-class organization.

Requirements

Master’s degree in a science-related field with 7-10 years of experience in pharmaceutical chemistry drug product/substance testing
Knowledge of regulatory requirements (GMP/GLP)
Theoretical/practical experience with analytical techniques including pH meter, spectroscopy (UV, IR), chromatography assay/imps (HPLC/UPLC, GC, IC)
Experience with analytical method validations data review
Knowledge of USP/EP compendia and ICH guidance
Proficiency with laboratory software such as Waters Empower, LIMS, and electronic notebooks
Detail oriented, accurate, precise with strong math and organizational skills
Strong communication skills including verbal, writing, and presentation

Responsibilities

Ensure clients receive quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations
Apply GMP/GLP in all areas of responsibility as appropriate
Read and understand analytical procedures
Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs
Gain a technical understanding of the techniques in which review is being performed
Use MS Windows applications such as Excel, Word, Access, and Outlook email
Conduct all activities in a safe and efficient manner
Demonstrate and promote the company vision