<ul><li>To ensure cGMP compliance with regulatory and QMS requirements.</li><li>Preparation and Review of Annual Product Quality Review.</li><li>Handling of Deviation in Track wise including Preparation, Review and Compliance of deviation.</li><li>investigation Report as well as completion of deviation flow in Track wise.</li><li>Review and active participation in investigation of Market Complaints in area of operation.</li><li>To Perform and Monitoring IPQA Activities in Various area of operation in Solid Oral Dosage form.</li><li>To Perform Sampling In-Process, Finished Product for Exhibit, Validation and commercial Product.</li><li>To Perform Calibration of Various IPQA instrument and review of Calibration Record.</li><li>Handling of Team and to impart training to team members related to SOP in area of operation.</li><li>To ensure updating of area as per audit agenda and keep team up to date as per audit agenda.</li><li>Statistical Evaluation and Continuous Process Verification (CPV) of Products using Minitab.</li><li>Initial Assessment, Review and Trending of oversight observation in Area of Operation.</li></ul><p><br></p>

Executive Officer Quality Assurance Documentation