Formulation Research & Development Supervisor

To establish, maintain, and ensure the readiness of the Formulation R&D laboratory, including general formulation, oncology, and sterile injectable development facilities. To support the installation, setup, qualification, calibration, and trial operation of R&D laboratory equipment and instruments.

To execute formulation development, process optimization, scale-up, stability studies, and registration batch activities for oncology and sterile injectable products. To facilitate technology transfer of developed products from R&D to Production and support site transfer activities.

To evaluate the technical feasibility, formulation composition, manufacturing process, and cost of new products proposed by the Business Development team, including in-licensed and Contract Manufacturing Organization (CMO) products.

To ensure compliance with applicable GMP, GLP, GDP, data integrity, occupational safety, and product-specific handling requirements during all R&D activities. To perform trouble shooting of Existing products & Production support (whenever required).

Planning for Procurement of RM PM for Process optimization and Registration batches Preparation of MFC, PVP/POP & HTS. R&D observation sample stability monitoring. RM & PM Procurement follow up and Sample submission for testing after receiving. Technical support to store personnel for proper entry of RM/PM/RLD.

Blocked Material list Monitoring and supporting Store Personnel for FIFO. Education: B. Pharma / M. Pharma (Pharmaceutics) Experience: 8-14 Year experience in formulation research & technology transfer.