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.Education:
- B. Pharm B. Pharm - Required
- M. Pharm M. Pharm - Preferred

Experience:
- 5 years or more in 5 - 8 Years

Specialized Knowledge:Licenses:
Amneal is an equal chance employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.

📌 Executive, R&d Injectable Technology Transfer (Ahmedabad)
🏢 Amneal Pharmaceuticals
📍 Ahmedabad