Experience in QA Validation and QA Documentation. Change Control, Deviation, Manufacturing Unit. Vendor Management. Preparation of APQR. Exp in Sterile and Tablet, Capsule. Exp in USFDA, MHRA, Audit. Desired Candidate Profile: To review documents like APQR, Process Validation Records. Preparation of BMR and BPR as per the production planning. Preparation and Review of SOPs.