Senior Executive
Perform analysis of raw materials, intermediates, finished products, in-process samples, stability samples, and cleaning validation samples. Operate and troubleshoot analytical instruments including
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Perform analysis of raw materials, intermediates, finished products, in-process samples, stability samples, and cleaning validation samples. Operate and troubleshoot analytical instruments including
Perform analysis of raw materials, intermediates, finished products, stability samples, and cleaning validation samples using HPLC, GC, UV-Visible Spectrophotometer, FTIR, Karl Fischer, Dissolution, a
Monitor shop floor activities to ensure compliance with cGMP, SOPs, approved Batch Manufacturing Records (BMR), and regulatory requirements. Review Batch Manufacturing Records (BMR), logbooks, equipm
Execute API manufacturing activities as per approved BMR, SOPs, and production plans. Supervise shift operations involving reactors, centrifuges, dryers, filters, and other process equipment. Ensure
Execute batch manufacturing activities as per Batch Manufacturing Record (BMR), SOPs, and approved process parameters. Operate and monitor reactors, centrifuges, dryers, filters, blenders, and other
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process condi
Ensure compliance with cGMP, GDP, GLP, Data Integrity (ALCOA+), SOPs, and regulatory guidelines. Perform shop floor QA activities, including line clearance, equipment clearance, area clearance, and i
Execute API manufacturing activities as per approved BMR, SOPs, and production plans. Supervise shift operations involving reactors, centrifuges, dryers, filters, and other process equipment. Ensure
Principal Tasks &Responsibilities • Work allocation for sampling , analysis of finish products, returned goods and review of analytical data generated through LIMS / modules and report to Section H
Execute batch manufacturing activities as per Batch Manufacturing Record (BMR), SOPs, and approved process parameters. Operate and monitor reactors, centrifuges, dryers, filters, blenders, and other
Perform shop floor QA activities to ensure compliance with cGMP, SOPs, and approved manufacturing procedures. Review Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), logbooks, and ot
Production : • Supervision of production & maintenance activities of respective shift. • To ensure that every raw material used is of right quality (approved from QC, having reference Number) and qu
Perform preventive, predictive, and breakdown maintenance of API manufacturing equipment. Troubleshoot and rectify mechanical, electrical, and instrumentation faults to minimize downtime. Maintain r
Perform and review analysis of raw materials, intermediates, finished products, in-process, stability, water, and cleaning validation samples as per approved specifications and test methods. Operate,
Implement and monitor EHS policies, procedures, and safe work practices across the plant. Ensure compliance with applicable statutory requirements, including Factories Act, Pollution Control Board re
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and approved SOPs. Monitor critical process parameters and ensure compliance with process specifications. Operate and su
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process condi
Perform chemical analysis of raw materials, intermediates, APIs, stability samples, and finished products using approved analytical methods. Operate and maintain analytical instruments such as HPLC,
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and approved Standard Operating Procedures (SOPs). Operate and monitor reactors, centrifuges, dryers, filters, blenders,
Lead and maintain the site Quality Management System in compliance with cGMP, ICH, WHO, USFDA, EU GMP, and other applicable regulatory requirements. Review and approve SOPs, specifications, protocols
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