August 2025

MSc / B.Pharmacy ; 9-12 years of experience in FG/ Stability/PM / GLP / Micro /D0C-QMS

Knowledge of QMS & compliance, qualification & validation, aseptic core monitoring and IPQA.

To Review, check the method validations data as per the USP 1225– Validation of Compendial methods, ICH-Q2 guidelines for validation of analytical procedures, ANVISA, ORA-LAB, SOP and method of analysis.

Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world

Regulatory Submissions: Prepare, submit, and manage regulatory filings for API products, including new drug applications, amendments, and variations, while ensuring compliance with relevant guidelines and reguiations.API Equipment Handling.

MD or equivalent medical degree required. Advanced knowledge and clinical training in a medical/scientific area (e.g., internal medicine / pharmacology etc.) with medical council certification required.

Masters in any branch of Life Sciences with three years of post-qualification experience in virology, molecular biology and BSL3 experience.

M.Sc in Life Science / M.Pharm from recognized University or Equivalent with NET/GATE qualified. National Institute for Interdisciplinary Science and Technology

BPharm/ MBBS/Integrated BS-MS/ MSc/ or equivalent degree, Dept, of Systems and Computational Biology, School of Life Sciences, University of Hyderabad