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Cipla in Goa, India, is seeking a production professional to monitor and execute capsule production activities during the shift while upholding cGMP and safety norms to meet targets.
The role involves managing resources, maintaining process parameters, and preparing manufacturing records in line with BMRs and quality requirements. Safety and compliance are emphasized throughout the shift.
Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets