Review analytical documents, raw data, STPs, and laboratory records to ensure compliance with cGMP and regulatory requirements. Hetero, B.Pharm, M.Pharm, M.Sc Chemistry Apply
Responsible for review of User Requirement Specification, Design Qualification, FAT Protocols. SAT Protocols, Installation Qualification, Operational Qualification, Performance Qualification Protocols and reports
Hetero is one of worlds leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with presence in 140+ countries and backed by 30 years of experience in the pharma sector.
Support Medical Affairs objectives for assigned Cardio-Diabetes / Specialty therapies in emerging markets. Provide scientific and clinical inputs using current guidelines, clinical data, and real-world evidence.