Parveen Shaikh Email and Phone Number

8+year experience in Quality Assurance department in pharma industry.Review of Analytical method validations.Review of Analytical documents like Specification and STP of Raw material and finished products. Handling QMS documents.Review of Instruments calibration data.Review of instruments and equipments for qualification data.Review of Product development Report as pr QbD .Review Packaging specifications and STPs,MPR.Review of formulation documents like Input specifications,MFR, stability protocol, admixture study protocol, procurement package, purchase requisition,PDR review and TTD submission.Preparation and review of SOPs for respective departments.Test licence and manufacturing licence maintenance for CFT'S.Trainings to new joinees.Support to RA for queries related to validations.