About the Role
Position Summary:
This role is responsible for Site Engineering activities for USFDA site with Injectable background and Qualification in Electrical Engineering.
Key responsibilities:
1. He is authorize to sign (as a doer / reviewer / verifier)
A. Engineering GMP Documents
B. Break Down / Preventive Maintenance Report
C. Qualification Documents.
D. QMS document review and closing.
E. Any other documents related to QMS.
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