Quality assurance role at Meril Life Sciences (USFDA – MYVAL): the person maintains and reviews quality documentation, handles CAPA, deviations, change control and non-conformances, and supports internal audits and regulatory inspections, ensuring compliance with USFDA, GMP and ISO 13485. Requires 1–3 years in the medical device/pharma industry and a B.Pharm/M.Pharm/B.Sc./M.Sc.
Sign in to see your match