Subhash Adaveni
About Subhash Adaveni
Subhash Adaveni is a Senior Associate in Quality Assurance at Ingenus Pharmaceuticals, where he has worked since 2016. He holds a Master of Pharmacy and has over four years of experience in quality assurance for sterile injectables manufacturing.
Work at Ingenus Pharmaceuticals
Subhash Adaveni has been employed at Ingenus Pharmaceuticals since 2016, initially as a QA Associate and later promoted to Sr. Associate - QA in 2019. He operates from the company's facility in Denville, NJ. His responsibilities include conducting online monitoring of aseptic operations in the Aseptic Processing Area (APA) and class 100 area. He is also responsible for internal document approvals, which encompass batch records, CAPAs, SOPs, and change controls. Additionally, he initiates investigations and manages deviations related to manufacturing processes, ensuring compliance with regulatory standards.
Education and Expertise
Subhash Adaveni holds a Master of Pharmacy degree in Medicinal and Pharmaceutical Chemistry from S R M University, where he studied from 2008 to 2010. He also earned a Bachelor of Pharmacy (B.Pharm.) from Rajiv Gandhi University of Health Sciences, completing his studies from 2002 to 2007. His educational background provides a solid foundation for his expertise in quality assurance, particularly in sterile injectables manufacturing, where he has over four years of specialized experience.
Background
Before joining Ingenus Pharmaceuticals, Subhash Adaveni worked at Gland Pharma Limited as a QA Executive from 2011 to 2015 in Gandimaisamma, Hyderabad. His role involved ensuring compliance with quality assurance standards in the manufacturing of sterile injectables. This experience contributed to his knowledge and skills in quality management and regulatory compliance, which he has further developed in his current position.
Achievements
In his current role, Subhash Adaveni participates in the site's internal audit program and supports preparations for external audits. He ensures that Good Manufacturing Practices (GMP), Quality, Health, and Safety are integral to all aspects of his work. His hands-on monitoring of production and non-production activities allows him to provide timely feedback on compliance issues, enhancing the risk management capabilities of the operational and functional areas he collaborates with.