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Vacancy for M.Pharm, B.Pharm in Technology Transfer at IPCA Laboratories


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Vacancy for M.Pharm, B.Pharm in Technology Transfer at IPCA Laboratories

IPCA LABORATORIES LIMITED is an Indian multinational pharmaceutical company. It produces more than 150 formulations that include oral liquids, tablets, dry powders, and capsules and sells these formulations domestic and global market. For more than 60 years, Ipca has been a crucial healthcare partner in over 120 countries across the 6 continents. We are a fully-integrated pharmaceutical company that manufactures over 350 formulations and 80 APIs for various therapeutic segments.  Today, we are one of the world’s largest manufacturers and suppliers of over a dozen APIs.

Post : Manager / Sr.Manager

Department : Technology Transfer
Qualification : B.Pharm/ M.Pharm
Experience : 10 to 15 years experience in tech transfer activities of solid oral dosage forms for regulated market.
Industry Preference : Pharmaceuticals Formulations

Job Responsibility
• Experience of managing team of 15 to 20 scientists, documentation officers and technicians
• Responsible  for planning and execution of scale-up and Exhibit batches of solid oral dosage forms for regulated market (EU, ROW and Canada etc).  
• Responsible for on time initiation of stability studies of exhibit batches.  
• To manage and maintain technical service area (Pilot batch area).  
• To  review all documents relevant to scale-up and Exhibit batches execution  like BMR, BPR, Protocols, scale up report, exhibit batches report and to provide filing documents to RA.  
• To co-ordinate with cross functional team like site manufacturing team (Production, QA and QC), R&D, RA, PDC, Supply Chain etc. to meet aggressive timeline for regulatory submission to meet business priorities.  
• To review, approve and effective implementation of change control proposal, deviation/Incident and CAPA for scale up and exhibit batches.  
• To evaluate and respond to deficiency of drug product by regulatory agencies.  
• Support production department for validation batches and trouble shooting of commercial batches.
• Perform job responsibilities in compliance with cGMP, SOP’s and all other regulatory agency requirements, where applicable

Request to share CV on with subject line "CV for TT"for  further scrutiny and shortlisting.

Last Date : 31st December, 2023

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