Job description
• Develop and maintain policies, procedures, and SOPs for drug manufacturing licenses.
• Prepare, review, approve, and distribute production instructions for all products in compliance with established procedures and SOPs.
• Oversee production planning, monitoring, and control of all products according to documented procedures and SOPs.
• Review all production batch records to ensure they are completed and signed.
• Report and evaluate production deviations, investigating critical deviations and documenting conclusions.
• Ensure all documentation is up-to-date and entries are made as required.
• Maintain cleanliness and, when necessary, disinfect production facilities to control environmental and microbial conditions in clean rooms and other areas according to SOPs. Ensure all records are maintained.
• Ensure timely material flow and availability of materials or semi-finished goods for subsequent processing stages.
• Monitor and verify the identification status of processes, materials, semi-finished goods, machines, and equipment at each stage.
• Analyze and reduce rejection rates at various process stages through effective monitoring, analysis, and root cause elimination.
• Review and implement SOPs and other documents as needed.
• Coordinate with supporting departments such as Engineering, QA, QC, Stores, and Warehouse.
• Monitor the validation and calibration status of processes, equipment, and measuring devices, ensuring all related protocols and reports are reviewed and approved.
• Investigate market complaints and take corrective actions as necessary.
• Attend organizational meetings to discuss production issues.
• Provide training to subordinate staff.
• Ensure the safety and health of personnel, taking prompt action in emergencies.
• Work on enhancing productivity, cost savings, and process improvements.
• Report functionally as per the departmental organogram.
• Perform any other tasks assigned by the Reporting Manager and/or senior management.
Job Type: Full-time
Pay: ?25,000.00 - ?40,000.00 per month
Benefits:
• Health insurance
Schedule:
• Day shift
Ability to commute/relocate:
• Visakhapatnam, Andhra Pradesh: Reliably commute or planning to relocate before starting work (Preferred)
Application Question(s):
• Do you have past experience in drug manufacturing?
Education:
• Bachelor's (Required)
Experience:
• total work: 3 years (Required)
Work Location: In person
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