Implement Operate monitor and maintain Quality Systems which enable operations on site to occur in an efficient manner and in compliance with Global Quality Standards and cGMPs. Review and ARchival of Quality System Documents Followup for timely closure of QMS docs Participating in the investigations analysis for Deviations, OOS, OOT, Compliants and Audit finding, morevoer responsible for providing batch disposition as per the outcome of Deviation, OOS and OOT investigations Supporting in external audits preparations and responding to audit findings Compliation of the Internal Audit response and follow up Assist in scheduling and preparation of management review meetings Organize the CAPA meeting, coordinate amange CAPA efforts and interact with customers to conduct compliant investigations Handling of Change Management CAPA Management System Assist to author , review and update quality procedures as applicable Responsible for Handling of Compliants, Mock recall/ Recall and withdrawal of Drug Products Retentions Sample Management Preparations of APR / PQR
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