Description
Duties include:-Reviews and approves GMP controlled documents including standard operating procedures.
-Leads the site Material Review Board.
-Issues batch records and labeling in support of immunotherapy manufacturing.
-Provides for batch record review and disposition of immunotherapy products.
-Performs lot packet review and disposition of raw materials.
-Ensures initiation, investigation, and closure of lot related deviations, non-conformances, and CAPAs.
-Provides support for the recall of non-conforming materials, investigations associated with product complaints, and biological product deviation reports.
- Hires and supervises the Quality Assurance staff that covers multiple work shifts.
Please be in contact as soon as possible for this urgent position!
To find out more about Real please visit www.realstaffing.com