Dr G.V SATYANARAYANA

Lead R&D operations, managing 3 group leaders and 20-member scientific teams.  Manage synthesis of drug intermediates, impurities, metabolites, deuterated molecules, and labelled isotopes.  Coordinate with clients on custom synthesis projects and ensure compliance with quality standards.  Supervise analytical chemistry support for structural confirmation and purity assessment

Managed a 10-member research team focused on drug impurities and intermediates synthesis.  Delivered multiple impurity reference standards for regulatory submissions.

 Directed 20 chemists across 3 groups in advanced synthesis projects.  Specialized in the preparation of isotopically labelled standards for pharma clients.

 Led a team of 10 chemists in drug impurity synthesis and analytical support.

 Executed synthetic projects for Tenofovir, Ezetimibe, Valganciclovir, Rizatriptan, and Propafenone.  Supervised drug stability and impurity profiling studies.  Trained and mentored junior chemists in advanced organic synthesis and analytical methods.

 Contributed to synthetic organic chemistry projects for clients, including Nektar and Virochem.

 Worked on collaborative research projects for AstraZeneca, Pfizer, Merck, and Boehringer Ingelheim.  Synthesized building blocks, scaffolds, and analog libraries for medicinal chemistry programs.