Qa Specialist
Current1.To ensure the CGMP compliance for documents.2 . Review of Executed BMR/BPR of commercial and exhibit batches for batch release.3.Preparation and updating of master formula record (MFR) and validation of documents of all dosage forms.4. To maintain art work approval sheet and shade cards.5. To prepare standard operating procedures.6. Responsible for Preparation of site master file (SMF), Updation of its Annexure as per requirement.7. To prepare elemental impurities risk assessment, Nitrosamine impurities risk assessment, Excipient risk assessment reports.8. In-process Quality Assurance during production/packing activities