Meeting the market requirements as per the schedule, maintaining the quality systems in the blending and filling areas as per the norms of the organization, coordinating with concerned departments for effective planning and functioning, training and developing an efficient team to ensure delivery as per schedule and implementation of cGMP practices to meet the Schedule M requirements and other regulatory as per the requirements of the organization.
Should be involved in similar operations nothing less than parenteral production preferably vaccines for a period of minimum 15 years and should be well versed with the requirements of NRA. He should be leading a team of professionals in a reputed firm and reporting to the senior management. Exposure to any international audits like MHRA, USFDA, WHO etc is required. Knowledge in packing materials will be additional qualification.