Senior Research Associate

• To prepare BOM for new UID activities with respect to costing of NPDs. • Timely development and delivery of allotted formulations and any other assigned project as per agreed timelines and budget. • Completion of document preparation and formulation activities to support pre-clinical, clinical supplies and technology transfer, exhibit batch manufacturing of developed product. • Development of non-infringing strategies for novel formulations in compliance to regulatory requirements for US, EU, and ROW market. • To write Lab note books, stability data compilation and tracking of project progress. • Preparation and request of spec for raw material, packaging material, in-process controls and finished product specification. • Preparation/review of documents for manufacture exhibit/ commercial batches like master formula card, product specifications, product development report and technology transfer docket and co-ordination with support functional team for timely delivery of projects. • Identification of product/Process specific equipment’s/ machinery and record keeping of usage and maintenance. • Ensure compliance of SOP’s, GLP, and GDP in product development of group.

Cadila Pharmaceuticals