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This role serves as a key contributor to regulatory operations by ensuring the accuracy, integrity, and compliance of regulatory information used for global submissions, registrations, product maintenance, and post-market activities.

Line management responsibilities for staff members. For direct and indirect reports, may participate in and manage activities related to department staff operations such as interviewing and selection, job description preparation, professional development

Perform setup activities including CRF creation, edit check specification creation, and User Acceptance Testing.

Exposure of handling manufacturing activities of OSD manufacturing activity (Granulation, Compression, Coating and Packing)

Formulation and process development activities for parenteral pharmaceutical products. Pre-formulation, compatibility, stability and optimization studies.

Sun Pharma is India’s No. 1 pharmaceutical company and a leading global player in specialty medicines. With over 40 manufacturing facilities and a diverse portfolio, we deliver high-quality medicines across 100 countries

Supervise and coordinate manufacturing operations in Oncology production areas. Manage Granulation, Compression, Coating, and Packing activities.

Testing & Method Validations; Culture Handling, Water & Bioburden Testing; Raw Material and BET Testing Water, Finished and Stability samples, Autoclave, Sterility Testing & observation of canisters.

To support and execute Analytical Method Validation activities, ensure data integrity and regulatory compliance for API products at our Udaipur API Plant.