Posted:6 hours ago|
Platform:
Work from Office
Full Time
Authorize to prepare and review the following documents:
a. Trial Batch /Development Batch Manufacturing Record.
b. Trial Batch / Scale up batch protocol & report.
c. All other documents (If any) from R&D and other locations
2. Responsible for monitoring of Trial / Development / Scale up / Exhibit batches to be executed in manufacturing area.
3. Responsible to coordinate with CFT members for preparation of production plan related to Trial/Development/Scale-Up/Exhibit batches.
4. Responsible to maintain the area with GMP compliance.
5. Responsible for handling of new products from R&D and other locations
6. Responsible for handling of technical issues/OOS/Deviation investigation related to ongoing products.
7. Responsible to prepare response related to filling of products.
8. Responsible to prepare/check the inventory for raw material and new change
Mankind Pharma
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