Senior Research Associate
Key Responsibilities A. Analytical Method Development & Optimization Develop, optimize, and establish analytical methods for pharmaceutical formulations and development samples. Perform analyti
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Officer
Execute batch manufacturing activities as per Batch Manufacturing Record (BMR), SOPs, and approved process parameters. Operate and monitor reactors, centrifuges, ANFD, dryers, filters, and associated
Senior Executive
Execute manufacturing operations as per approved Batch Manufacturing Records (BMR), SOPs, and production plans. Supervise shift activities and ensure timely completion of production batches. Handle
Senior 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
Officer
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and SOPs. Monitor and control unit operations such as charging, reaction, filtration, centrifugation, drying, milling, bl
Officer
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and SOPs. Monitor and control unit operations such as charging, reaction, filtration, centrifugation, drying, milling, bl
Technical Assistant
• Ensure the c-GMP Compliance and schedule M compliance in production. • Ensure the completion of production targets with zero quality issue. • Ensure the compliance of inspection /Audit in coating
Officer
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and SOPs. Monitor and control unit operations such as charging, reaction, filtration, centrifugation, drying, milling, bl
Assistant Manager
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 conditions
Technical Supervisor
1. Ensure the cGMP compliance of packing area Key Responsibilities: • Follow up of Standard operating procedure. • Follow up of Current Good Manufacturing Practices. • Completion of Online Doc
Officer
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and SOPs. Monitor and control unit operations such as charging, reaction, filtration, centrifugation, drying, milling, bl
Executive
"1. Planning and execution of Validation, Qualification, Re-Qualification and Re-Validation activities pertaining to Manufacturing facility at Dholka site in line with the cGMP requirements of nationa
Apprentice
Role Objective / Major Purpose of the Job The Quality Assurance (QA) Apprentice is responsible for supporting quality assurance activities to ensure products are manufactured in compliance with cGMP,
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
Executive
Receive and verify incoming raw materials against Purchase Orders and Goods Receipt Notes. Ensure proper unloading, identification, labeling, and storage of materials as per SOPs. Maintain FEFO/FIFO
Technical Supervisor
Major Purpose Of The Job:- To review Daily Packing plan for the assigned Packing line activities. To ensure that arrangement of dispensed batches for the day in advance. To ensure that Daily/Weekl
Officer
Perform preventive, predictive, and breakdown maintenance of field instruments and control systems. Maintain process instruments such as pressure, temperature, flow, level, pH, conductivity, differen
Senior Officer
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
Assistant Manager
Develop, implement, and monitor EHS policies, SOPs, and safety management systems. Ensure compliance with the Factories Act, State Factory Rules, Pollution Control Board requirements, Hazardous Waste
Senior Executive
Major purpose of the job: Preparation of DMF, annual update and its submission to various regulatory authorities. Preparation of Applicant's part CEP/DMF/ASMF and responses of various Applicant's pa
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