About this role
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