Literature search and patent review of products. Responsible for formulation development of DPI & pMDIs formulations for US, EU, ROW, CSI and IRF markets. Responsible for planning and execution of development- Pilot / Scale-up and Exhibit activities for pulmonary formulations. Responsible for preparation and compilation of project related documents in compliance with quality and regulatory requirements. Responsible for lab maintenance and upkeep of the laboratory and equipment’s. Responsible for analytical data and interpretation for way forward. Responsible for Coordination with planning, engineering department and purchase department for product related activities. Responsible for Preparation of department SOPs, guidelines, product related protocols and tech transfer documents along with DQA, CQA and regulatory team.
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Job Type
Full-time
Education Level
Ph.D. or professional degree