Executive / Sr. Executive: QA - QMS @ HP

1. Documentation, QMS Documentation, Validation, qualification, deviation, change control etc
2. MFR/SOP/AMV (analytical Method Validation), ACTD/CTD, Dossier Preparation.
3. Knowledge of COPP.
4. Having a sound knowledge of BMR preparation and filing, FR&D Documentation, PV ETC Monitoring of process validation activity with preparation of protocol and report.
5. Monitoring of cleaning validation activity with preparation of protocol and report.
6. Review the Qualification document of equipment and facility.
7. Review of instrument and equipment calibration.
8. Review and monitoring of Revalidation of process and requalification of equipment/instrument.

Industry Preferred: Pharma company only in pharma formulation of oral and solid.