Senior Research Associate-FD

Formulation development of NCE projects, generic projects and line extension projects

Preparation/review of literature summary and development report to the assigned product.

Involve in execution and/or supervision of formulation development, process development and manufacturing of GMP batches of assigned product.

Preparation/review of technical documents, which includes but not limited to MFC, BMR, BPR and Stability protocol following GDP.

Representation in departmental audit

Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same.

Execution and/or supervision of scale up/pilot scale batches in pilot plant under GMP condition.

Preparation and/or review of technology transfer documents and technology transfer to manufacturing site, whenever required.

Preparing/reviewing of QMS includes but not limited to change control, deviation, SOPs and OOS

Communication with cross-functional team and client via mails, meetings and oral communication