1) - Documentation, QMS Documentation, Validation, qualification, deviation, change control etc
2) - Monitoring of process validation activity with preparation of protocol and report.
3) - Monitoring of cleaning validation activity with preparation of protocol and report.
4) - Review the Qualification document of equipment and facility.
5) - Fill up the vendor questionnaire, handling and conducting of vendor qualification/audit.
6) - Review of instrument and equipment calibration.
7) - Review and monitoring of Revalidation of process and requlification of equipment/instrument.
8) - Assigning of self life of finished product as per stability data.
9) - Review of preventive maintenance schedule.
Posted By Consultant