Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Life has always been and continues to remain, our guiding purpose. Driven by the same purpose, we have extended our presence to 80+ countries providing over 1,500 products across various therapeutic categories in 50+ dosage forms. To make healthcare more affordable globally, we are deepening our presence in the key markets of India, South Africa, the U.S. among other economies of the emerging world.
Post : Shift In-charge - Production
Job Purpose
Monitor the production activities in a shift by maintaining cGMP and safety norms to achieve production targets
Key Accountabilities (1/6)
• Monitor production activities in a shift by managing available resources to achieve production target
• Monitor planned production activity to meet production targets for a shift Utilise shift resources optimally to get desired production output
• Regulate usage of consumables in the production process at optimum levels to save costs
Key Accountabilities (2/6)
• Maintain and monitor standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality
• Ensure all operations are performed as per GMP & Safety norms by reviewing all processes and documents for compliance
• Ensure equipment, facility and block premises are maintained as per regulatory compliance
• Maintain system integrity by updating documentations and deviations on CipDox while performing operations
• Perform validation, qualification and calibration as per schedule and update output of all activities in the systems
• Conduct training related to equipment handling, unit operations, unit processes, documentation, cGMP for operating staff
• Participate during the preparation of SOPs, FMECA (risk analysis) and submit for review
• Prepare new documents and update existing documents as per GMP requirement
Key Accountabilities (3/6)
• Prepare manufacturing records and update online documentation to meet production and cGMP requirements
• Maintain online documentation and timely entries in BMR and supporting documents
• Prepare new documents and update existing documents as per GMP requirement
• Operate software such as SAP, CipDox and QMS
Key Accountabilities (4/6)
• Ensure that safe work processes are followed and safety appliances are utilised during production activities in shifts to create a safe working environment
• Ensure safety systems and procedures followed in the shift
• Ensure availability and usage of PPEs in the shift by coordinating with HSE department for requirements and shift schedule
• Ensure compliance to safety training targets by monthly reconciling attendance records
Key Accountabilities (5/6)
• Identify the deficiencies/errors and propose new ideas and suggest improvements to reduce the complexity in processes
• Identify the deficiency in area and errors in documents and rectify them as per requirement
• Propose and implement new idea to enhance production, optimise the use of consumable goods and maximum utilization of resources
Candidate Profile
Bachelor in Pharmacy
5-6 years of experience with 2-3 years of experience in pharmaceutical manufacturing Knowledge of cGMP practices, equipment operations required for Formulation Production
Additional Information
Experience : 5-6 years
Qualification : B.Pharm
Location : Rangpo, Sikkim
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 20th March 2026
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