Executive
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
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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
"• To perform vendor management activity to assure that vendors are complying with Cadila procedure on vendor management and GMP requirements in order to source quality materials and product
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packi
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
Maintenance Services : • To distribute the daily work to technician as per plant & Utility job request & ensure timely compliance. • To co-ordinate with electrical, instrument and Utility person for
Preventive Maintenance : • Preventive maintenance of the equipment’s is as per checklist and instruction / Feedback from Section -Incharge. • Prepare preventive Maintenance Checklist for all the pl
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
Participate in investigations related to OOS, OOT, deviations, incidents, and CAPA implementation. Support method validation, method transfer, cleaning validation, and stability studies. Assist duri
"To perform In-process Quality Assurance for the process / products being manufactured and packed in Main Pharma Block (Tablet / Capsule). To ensure Quality and cGMP compliance of the products being
Review Batch Manufacturing Records (BMRs), Batch Packing Records (BPRs), logbooks, and other GMP documents for completeness, accuracy, and compliance. Ensure timely review and disposition of manufact
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
• 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 conditions for batc
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packi
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
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 routine shop floor monitoring to ensure compliance with cGMP, SOPs, and data integrity requirements. Verify line clearance activities before batch initiation and monitor critical manufacturin
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packi
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 analysis of raw materials, intermediates, finished products, stability samples, and utilities as per approved specifications, test methods, and pharmacopoeial requirements. Conduct chemical a
• Review of validation documents (Mfg. Process, Cleaning, equipment and water validation etc.) and overall monitoring of validation activities. • Responsible for Document Data Control. • Internal Au
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