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2.0 - 6.0 years
0 Lacs
ahmedabad, all india
On-site
You will be responsible for the development related activities of all Parenteral Products. This includes preparation and review of MFR for exhibit batch of Parenteral products, indenting the raw materials, RLD, Packaging Material, and other items required for product development and exhibit batches. You will also be in charge of preparing and reviewing study protocols required for exhibit batch of parenteral products, reviewing specifications like API, Excipients, In-process, finished product, Shelf life etc. of Parenteral products, and primary packaging material. Additionally, you will review BMR and BPR of Exhibit batch, support Regulatory affairs department for ANDA submission and respond...
Posted 2 weeks ago
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