walk in jobs

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

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.

Diploma in Pharmacy from a recognized University/Institution and must be registered Pharmacist under Pharmacy Act 1948

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

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.

Planning and performance of Validation, Verification of analytical methods as per the relevant procedures, protocols.

B.Sc., M.Sc., B.Pharm, M.Pharm; Cliantha QC Lab Reviewer and QA Lab Auditor. Research QC ensures compliance with regulatory standards by maintaining the quality of data for both small and large molecule bioanalytical laboratories.