Post : Assoc Dir R&D Unit
Job Description
• Formulation development of solid oral dosage form.
• Supervise and guide the team for development activities as per SOP.
• Monitoring Key milestones of products under development.
• Review of Developmental strategies & Patent summary prepared by subordinates.
• Coordination with inter and intra departments, planning & execution of the development activities as per regulatory requirement.
• Coordination with cross functional teams and aligning their priorities
• To monitor & ensure timely preparation and approval of various documents pertaining to Formulation research development department.
• Review and approval of tentative specifications for Raw material/ Packing material/In-process/ finished product.
• Review and approval of MMF.
• Coordination and supervision of bio batches manufacturing.
• Coordination with Bio-pharm. team and evaluate the Bio study results.
• Review and approval of Developmental reports and data for dossier.
• Training & development of self and subordinates. Team building and on the job training for the scientists from time to time.
• Implementation of QbD principles at development and scale up stage.
• Identification of project needs at the inception of projects
• Project tracking, management, risk assessment and contingency plans
• Strategy building, patent landscape, development methodology, business case, project cost for each project
• Formulation development of solid oral dosage form.
• Supervise and guide the team for development activities as per SOP.
• Monitoring Key milestones of products under development.
• Review of Developmental strategies & Patent summary prepared by subordinates.
• Coordination with inter and intra departments, planning & execution of the development activities as per regulatory requirement.
• Coordination with cross functional teams and aligning their priorities
• To monitor & ensure timely preparation and approval of various documents pertaining to Formulation research development department.
• Review and approval of tentative specifications for Raw material/ Packing material/In-process/ finished product.
• Review and approval of MMF.
• Coordination and supervision of bio batches manufacturing.
• Coordination with Bio-pharm. team and evaluate the Bio study results.
• Review and approval of Developmental reports and data for dossier.
• Training & development of self and subordinates. Team building and on the job training for the scientists from time to time.
• Implementation of QbD principles at development and scale up stage.
• Identification of project needs at the inception of projects
• Project tracking, management, risk assessment and contingency plans
• Strategy building, patent landscape, development methodology, business case, project cost for each project
Additional Information
Qualification : M.Pharm, Ph.D
Location : Goa
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : R&D
End Date : 25th May, 2019
Qualification : M.Pharm, Ph.D
Location : Goa
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : R&D
End Date : 25th May, 2019
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