Posted:1 day ago|
Platform:
Work from Office
Full Time
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
-M. Pharm
Piramal Pharma Limited
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