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1. Directs, through intermediate subordinates in inspection and testing activities to ensure continuous control and right sampling, testing and to approved or reject of all starting materials, packaging material, intermediate, bulk and finished products. 2. To execute and implement current Good Lab Practiced (cGLP) and ensure that its strictly followed and the adaptability to current Good Manufacturing Practices (cGMP). 3. To monitor and ensure all the QC records are evaluated and signed by an QC authorized person before they are send to the QA Department. 4. Heading all Quality Control (QC) functions and ensuring that all necessary tests are carried out in accordance with valid analytical protocol as per approved specification. 5. To monitor the maintenance, safety and housekeeping of QC labs, staffs, premises and equipment. 6. To ensure that initial required and continuous training and evaluation to personnel is carried out and adapted accordingly when needed. 7. To supervise all activities related to analysis and Stability studies of Finished Products in coordination with QA and R&D. 8. Involved in approval and monitoring of suppliers of raw material and packaging material as per the supplier evaluation audit. 9. Prepares, reviews, follows, monitors and record all QC SOP’s, Risk Assessment and Specifications in compliance with cGLP. 10. To ensure, prepares, monitors and document all required appropriate validations are done.