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Description: Job Description - Review of various quality system documents. - Preparation and review of Standard Operating Procedures. - Handling of QAMS activities like change control, OOS, OOT, Deviations, Lab Incidences and CAPA etc. - Preparation and review of quality risk management. - Review of batch manufacturing record and batch packing records. - Review, assessment and closure of other QAMS documents whenever required. - Review of validation and qualification documents. - Handling of market complaint and participate in investigation. Work Experience 7- 10 years Education Graduation in Pharmacy Competencies