Bioreva Sciences Limited

Responsible for preparation of Revision of SOPs as per periodic review. Responsible for preparation of New SOP as per requirement. Responsible for preparation/revision of Site Master File (SMF), Validation Master Plan (VMP) & Quality Manual (QM). Responsible for handling of Market Complaints regarding any product & Response CAPA with records. Responsible for handling of Change Control as per requirement & maintain their Log book records accordingly. Responsible for handling of Deviation regarding any Product/Process during operation and customer end and maintain their Log book records accordingly. Responsible for review of Process Validation records, Qualification & Calibration records for any Product/Equipment as per requirement. (HVAC, Water System, Compressed Air & Production Machines) Responsible for review/maintenance of Vendor Qualification records. Responsible for Schedule Self-Inspection department wise and maintain the records accordingly. Responsible for Preparation of Training Schedule & maintain the training records accordingly. Any other task allotted by the senior. Job Type: Full-time Pay: ₹45,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Work Location: In person