Roles Responsibility:

To execute Pre-formulation studies, bench scale batches using different formulation processes.

To support and execute the tech transfer activities, pilot batch manufacturing and bioequivalence studies etc.

Coordination and correspondence for the arrangement of API, RLD, Excipients, Punches and other accessories for Lab scale batches.

Coordination with cross functional departments like RA, QA, QC and ARD.

Should have knowledge of Solid oral and liquid oral dosage form development.

Should have valuable knowledge of F RD equipment and their handling.

Responsible for conducting Literature search, Experimental batches, Pilot and Pivotal batches.

Should have exposure in patents and non-infringing development.

Must be able to prepare development documents like Master Formula Records (MFR/MPR), development protocols, and pharmaceutical development report.

Need to be develop the Products by QbD fashion and expertise in DoE studies and interpretation using competent software.

Willingness and Cooperation to work at Contract Manufacturing Organization (CMO) sites.

📌 Executive - Formulation - Research Development (Chennai)
🏢 Desirous Global Consulting
📍 Chennai