Preparation Master Formula Record, Batch manufacturing records, batch packing records, equipment cleaning records, and filling documents online as per cGMP requirement. Conteprenious wording /documentation. To carry out production activities in co-ordination with Head production. To maintain necessary documents (BPCR, equipment use log etc.) for manufacturing and supervising Production and related activity. Production API’s or intermediate according to SOPs and as per cGMP guidelines. Observe and implement safety system in the entire plant. To lead a team for ensuring safety in working. Proper allocation of manpower. To monitor production area activity and maintain it properly. Responsible for handling of production worked quality events,(change control, deviation, market complaint etc.) GMP, Quality & compliance safety and productivity in the respective shift. Material management on the shop floor,
