- Analytical Method Management: Oversee method development, validation, and transfer for OSD, Injectables, and long-acting formulations—with a strong emphasis on liposomal formulations and nano-suspensions.
- Regulatory-Driven Stability Studies: Design, execute, and monitor stability studies in strict alignment with global regulatory requirements.
- Advanced Solid-State Characterization: Perform and interpret complex analyses using spectroscopic techniques, PXRD, DSC, TGA, Zetasizer, and other physical characterization tools.
- Lab Compliance & GLP: Maintain rigorous Valuable Laboratory Practices (GLP) and ensure continuous audit-readiness and laboratory compliance.
- Hands-on QMS Management: Actively manage and execute Quality Management System (QMS) workflows, including investigations, deviations, change controls, and CAPAs.
- Training & Capability Building: Conduct technical training sessions for the team on analytical instrumentation, SOPs, STPs, and equipment operations.
- External Coordination & Outsourcing: Coordinate seamlessly with vendors, contract testing laboratories, and auditors to manage external analytical testing, compliance, and outsourcing activities.

📌 Sr. Scientist 1 (Karnataka)
🏢 Aurigene Oncology
📍 Karnataka