• Review of various quality system documents.
• Preparation and review of Standard Operating Procedures.
• Preparation and review of Annual product quality review reports.
• 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.
• Preparation and review of Standard Operating Procedures.
• Review, assessment and closure of other QAMS documents whenever required.
• Issuance and retrieval of SOP, various list, protocols and logbooks etc.
• Maintain all cGMP records.
• Management of control sample area.
• Review of validation and qualification documents.
2-5 years
Education Graduation in PharmacyCompetencies