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.
  • Conceptualize and Impl...

    • Apply for this Position

    Ready to join SUN PHARMA? Click the button below to submit your application.

    Submit Application