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To plan the development activities / process improvements and ensure robust and feasible transfer of manufacturing process technology for pharmaceutical oral dosage forms, in-house developed
Adherence to the project time lines, ensuring all compliance norms.
Formulation development , Exhibit and monitor all development activities of various solid oral dosage forms
Relevant expertise of 03 to 07 years in the field of process development (OSD Products)
Ensure compliance and process requirements for the Pilot / Scale-up and the Exhibit batches.
Plan/Document / Support / Coordination and Execution's of the scaleup / optimization manufacturing batches as per the plan
Provide feedback / support to bridge the process gaps and offer solutions to the complex issues and updates periodically to the team leader
Review and offer the recommendations to the process validation reports / protocols
Participate in planning of exhibit / submission batches
Requisite skill set:
Masters in Pharmacy (Pharmaceutics)
knowledge of regulatory guidelines / GMP norms
Strong technical acumen
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Date Posted: 20/10/2024
Job ID: 97055565