Job Title

Job Description1.Responsible for overall activities performed in the Quality Control Department. 2.Implementing and monitoring of cGLP norms in the Quality Control Department. 3.Responsible for internal/Customer/Regulatory Audits and Preparation of Reports. 4.Implementation, Compliance and Maintenance of Quality Control SOPs. 5.Responsible for Document Management System for Raw Material, In-Process Samples, Packing Material, Finished Product and Stability Samples. 6.Managing Deviations, Change Control, Incidences with Investigations and associated CAPA. 7.Investigation of OOS,OOT & OOE in the Quality Control Department and associated CAPA. 8.To review and approve the Validation/Qualification protocol and report of the equipment installed in the Quality Control Department. 9.Arrangements of Analytical Method Transfer, Analytical Method Validation of Chemical and Micro sections. 10.Accomplishing QC Human Resources objectives by Recurring, Selecting, Training, assigning, counseling and discipline employees. 11.Meet QC financial objectives by estimating requirements. 12.Involving in self inspection, CFT meeting and functional review meeting. 13.Achieving QC operational objectives by contributing information and analysis to strategic plans and review. 14.Review and approval of analytical documents w.r.t. Data Integrity. 15.Release/ reject of Raw Materials, Packing Materials, Stability,In-Process and Finished Products. 16.To impart trainings to the subordinated and participate in the training programs organized by the company. 17.To ensure that prescribed safety precautions are being taken by the subordinates while performing analysis