Venkatesh Reddy

Venkatesh supports TDP’s clients with technology transfer and process validation activities, working directly with client teams to help ensure projects are delivered effectively and in accordance with applicable quality and regulatory requirements. His role combines practical on-site support with technical oversight across complex pharmaceutical operations.

A qualified pharmacist and experienced Quality Consultant, Venkatesh has more than 15 years’ experience across Quality Assurance, Quality Control, New Product Introduction, auditing, validation, and Regulatory Affairs. His background also includes providing Qualified Person support for the importation, testing, and batch release of medicinal products for the EU market. He holds the qualifications and experience required to be eligible for QP status within the EU.

Venkatesh’s expertise spans both analytical and manufacturing environments, with a particular focus on small-molecule medicinal products. He has hands-on experience with analytical instrumentation, alongside a strong understanding of pharmaceutical manufacturing, technology transfer, process validation, and the quality systems required to support compliant operations.

He also has significant experience establishing pharmaceutical manufacturing and wholesale distribution operations. Venkatesh has successfully supported the development and approval of three Manufacturing and Importation Authorisations and one Wholesale Distribution Authorisation.

His combination of technical knowledge, regulatory experience, and practical delivery enables him to support clients through complex projects while maintaining a clear focus on compliance, quality, and successful implementation.