: Responsible for planning day to day activities in Production Department. Responsible for monitoring output of Production. Preparation of Daily Production Report. To take charge of operations from previous shifts Chemist/Officer and give charge of operations to next shifts Chemist/Officer. Allocating & managing the men power in Tablet Production Department as & when required. Performing I.P.Q.C. (In Process Quality Control) during the manufacturing of Tablets. Compliance of the requirement of cGMP. Co-ordination with Q.A., Q.C., Maintenance Department. To maintain safety, efficacy, quality and enhance quality during all Pharmaceutical operations. To manufacture all products with the compliance of respective Master Formulae Record. To ensure final completion of BMRs. Log Books & all other records on line and transfer to Q.A. To train the Workers & Operators regarding the SOPs on job training & evaluation of the same. Review of Standard Operation Procedures (SOPs) for the activities of Production Department
Employement Category:
Employement Type: Full time Industry: Others Role Category: ProductionQuality (QA-QC) Functional Area: Not Applicable Role/Responsibilies: Production Chemist