Roles and Responsibilities
- Execute production batches as per plan.
- Preferable from API Bulk drugs Industry.
- Must have Experience in USFDA approved site.
- Following relevant SOPs.
- Verification of cleaning area / equipment and completion of Logs.
- To comply with cGMP standard during the entire manufacturing activity.
- Concurrent completion of batch process records.
- To maintain the manufacturing facility as per the regulatory norms.
- To comply with EHS standards.
Time and venue
Interview Venue: Sai Life Sciences Limited, SLN Terminus, 4th Floor, Gachibowli Miyapur Road, Gachibowli, Hyderabad,view on map
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