Roles and Responsibilities Manage production planning, batch processing, manufacturing operations, and plant production to ensure timely delivery of high-quality products. Develop and implement effective strategies for improving productivity, reducing costs, and increasing efficiency in liquid manufacturing processes. Ensure adherence to regulatory requirements by maintaining accurate records of production activities and implementing corrective actions as needed. Collaborate with cross-functional teams to resolve issues related to equipment maintenance, personnel management, and supply chain logistics. Desired Candidate Profile 15-20 years of experience in pharmaceutical industry with expertise in Batch Processing, Manufacturing Operations & Management. Bachelor's degree in Pharmacy (B.Pharma). Strong understanding of GMP regulations and ability to apply them effectively throughout the production cycle. Confident on facing regulatory audits like USFDA, MHRA
Roles and Responsibilities Ensure compliance with GLP guidelines, including investigation of OOS/OOT events and vendor qualification. Maintain accurate records of GLP documents, instruments, and equipment through preventive maintenance schedules. Conduct calibrations on instruments according to CGMP requirements and perform spares management tasks. Implement LIMS system for effective inventory control and HPLC analysis. Perform CAPA activities as needed to resolve quality issues. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Organic Chemistry from a recognized university. Minimum 10-15 years of experience in pharmaceutical industry with expertise in GLP practices. Strong understanding of instrument calibration procedures under cGMP regulations. Proficiency in maintaining IQ, OQ, PQ documentation for laboratory equipment.
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