Rupinder Dhaliwal Email and Phone Number

Issuance /Submission & Review of BPR, QC Protocol. Preparation of COA, Product Labels. Archiving of documents Release of FG for Domestic/Export as per Market Requirement Trending of Quality Data and its Statistical evaluation. Compilation of Annual Product Review. Maintaining Log for Market complaint, Deviation, OOS, Change control. Performing IPQA Activities Looking after all the Quality process Review of Active Pharmaceutical Ingredients (API). Review of all Test protocol/Reports Reviewing BPR. Quality system Tracking (Change Control, OOS, Deviation & Market Complaints, CAPA). Vendor evaluation and new Vendor development/Assessment.Regularly documentation of Internal Quality Audits (member of SIP team). Preparation of Annual Product Review Monitoring all raw materials, Packing Material, intermediates and finished products analysis according to in house analytical standards set by R & D. Preparation & Implementation SOP /STP/BPR/Formats as per PDD Spec. Printing of FG labels, Planning & Release of Finished Product as per Market requirement. Project/Dissertation Project Work on Mutations (Genetics deptt) from Punjabi university, PatialaSummer Training on Microbiology from Verka Milk Plant, Ludhiana