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