Job Description & How to Apply Below
1.Perform Downstream manufacturing batch operation in cell culture manufacturing facility following cGMP and safety practices
2.Preparation of Buffers and solution required for Downstream batch execution
3.Qualification of new equipment and equipment qualification document preparation. Coordination with vendors for equipment error / troubleshooting.
4.Preparation and revision of equipment and process related SOPs , Batch record preparation and revision , Protocol & report preparation and revision .
5.Initiation of deviations, Change controls, CAPA, quality risk assessment, Investigation report preparation & closure of the QMS documents.
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