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M.Pharm / M.Sc ; 3-5 years of relevant experience in Quality Control department, Analytical Development Lab. Good communication, technical report writing skills and E- Mail etiquette.

Experience in Tablet and Liquid Packing & Manufacturing (Primary & Secondary, Good understanding of Track & Trace and Serialization Systems, Operational knowledge of Liquid Oral Formulations in the Packing Section

Responsible for Formulation Development of Nasals Formulations. Responsible for conducting Formulation Development Trials and documenting the details in LNB.

Handling large-scale bioreactors, Continuous centrifuge, filter integrity, aseptic techniques. Strong cGMP knowledge and data analysis skills

This role is key to maintaining accurate records, supporting production operations, and driving continuous improvement in documentation practices.

M.Pharm, B.Pharm, M.Sc, B.Sc Candidates must be open to work in shift duties and having pharma experience in regulated plant like USFDA, MHRA should apply.

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.

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