- Part of Technology Transfer Team (Under R&D vertical ) at Pipan location
- Responsible for Preparation of Master BMR, BPRs and document management.
- Responsible for coordination with various departments like Regulatory Affairs, Manufacturing, Warehouse, Quality Assurance, Quality Control, Engineering for execution of Scale-up and Exhibit batches.
- Responsible for reviewing GMP related documents.
- Responsible to select Equipment at Facility.
- To facilitate the Change Controls to be logged for various reasons. To initiate the Change Controls due to revision in BMR / BPRs and other PD related changes.
- To study critical parameters during scale up batches to optimize the CPPs and CQAs.
- To provide the input related to batch size, process feasibility & process parameters to formulation scientist as per requirement.
- To monitor and ensure readiness for execution of scale-up / feasibility batches, Exhibit batches with respect to RM, PM & Miscellaneous items.
- Responsible for reviewing GMP related documents as applicable.
- To get actively involve in Scale-up and Exhibit batches.
- Activities other than the defined in the Job responsibility are to be done, as per the requirement of HOD, by following HOD’s instruction and guidance.
B. Pharmacy / M. Pharmacy
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