Registered Pharmacy with more than 7.5 years of multi-disciplinary Industrial Pharmaceutical Experience.
A professional having knowledge of Product manufacturing in oral solid general as well as Cephalosporin Section, & in Liquid sterile area.
having knowledge of Risk Management System, Validations & Analytical procedures, Compliance, and audit/gap analysis as per GMP and overall in-process and documentation control.
Dealing with all the Validation Protocols & Reports (IQ, OQ & PQ), Cleaning Validation, Validation Master Plan, Site Master File etc
Documentation & In-process Control
Manufacturing of sterile batches and to look after all the process till the stock released for sale in market
supervision of all the manufacturing & packaging activities of the oral solid department. issuance of PO and completion of BMR