Job Description

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.

  • Handling of Halol-1 (Sterile) Engineering Operation, HVAC, Electrical and Facility Management related activity.

  • Preventive Maintenance approval, Instrument / Equipment inward approval, Qualification protocol and SOP review and approval.

  • Improvements to reduce the Break down time of Production Equipments.

  • To ensure all critical utilities as HVAC and Water systems are available round the clock as per requirement.

  • Conceptu...

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