Posted:3 days ago|
Platform:
Work from Office
Full Time
1. To procure Raw materials from Ware house
2. Carry out the manufacturing operations according to the BPCR provided by QA department
3. Perform the Operations in accordance to the established SOPs and cGMP and capture the data in relevant documents.
4. To maintain for Good documentation practise at work place ( ALCOA)
5. To ensure the entry of batch related details in ERP.
6. To execute batches every day as per the Production planning schedule.
7. To arrange for Quality testing of in-process, intermediate & finished goods as per SOP.
8. To execute Trial / Validation batches as per the specific steps mentioned in the concerned Protocol.
9. To maintaining good Housekeeping in and around the concerned Production area.
Apitoria Pharma
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