Officer

Job Description

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.

Work Experience

2-4 years

Education

Competencies