Preparation, review and execution of process validation protocols and reports for all regulatory markets.
Preparation, review and execution of cleaning validation protocols and reports.
Preparation, review and execution of hold time validation protocols and reports.
Handling of validation and stability samples.
Handling of HVAC validation and facility qualifications.
Temperature mapping of new and renovated facilities.
Handling of Equipment validation (Preparation of IQ, OQ and PQ protocols for both sterile and non sterile dosage forms ).
Review and updation of master validation plan.
Preparation of validation schedules.
Review of quality control reports related to validation of activities.
Preparation and review of stability protocols and stability samples.
Review of Analytical Method validation documents related to new products and cleaning validation.
Monitoring and maintenance of stability chambers regularly.
Dealing into Injectables.
Note-Candidates should be a Male person.