Preparation, review and revision of Standard Operating Procedure and Integrated QMS documents ensure training.
Verification of Implementation with respect to cGMP system for manufacturing operations
To support in Handling Regulatory and Non regulatory inspections.
To carry of Compliance action post audit.
To carry out self-inspections, issuance, review and their closure.
To review all executed quality related controlled documents like quality procedures, SOP’s, BMPR’s and specifications etc.,
Preparation and review of technical agreements.
Review and compilation of calibration, validation protocols and reports.
To perform vendor qualification , Review Vendor Qualification set and preparation of vendor list.
Archival and retrieval of documents.
Verification of control documents, issuance and their retrieval.
Preparation, review, compilation and execution of PQR.
Handling of change control and deviations, issuance, review and their closures.
Handling of corrective and preventive actions, issuance, review and their closure.
Assignation of numbering system to BMPR.
To carry out in process Quality Checks.
Handling of market complaints, investigation, completeness and closure.
Vendor Qualification data verification and generation of item codes.
To arrange and provide departmental trainings as per Training Calendars.
To perform the Job assigned by Dept. Head in absence of Officer in the QA Dept., if any.
Mylab Discovery Solutions Pvt. Ltd., is an Indian diagnostic company that, develops & commercializes tests used in human diagnostics, food safety, agriculture, and veterinary medicine, empowering labs to obtain reliable, timely, and actionable results.