SU

Senior Manager Production Injectables

Sun Pharma
Kolkata5-11 LPA Posted 28 Apr 2025
FULL TIME
Qms
Gmp
Sub
Formulation
Usfda
+1 more

Job Description

He is responsible for Vial Filling Line, PFS Filling Line, Infusion bag line and API line Manufacturing area and Autoclave area, aseptic area, Freeze drying area, qualification / re-qualification activities in Parenteral manufacturing Area (Block-E).

Areas of Responsibility

  1. He is authorize to sign ( as a doer, reviewer & Approver ):
  2. Parenteral GMP documents
  3. Breakdown memo perform impact analysis
  4. Equipment and Area cleaning/sanitization logs
  5. He is responsible for overall QMS activity.
  6. Involved in the equipment Qualification / Re-Qualification activity in parenteral Manufacturing area (Block-E).
  7. He is responsible for activities related to parenteral Manufacturing area (Block-E).
  8. He is responsible for Vial Filling Line, PFS Filling Line, Infusion bag line and API line Manufacturing area and Autoclave area, aseptic area, Freeze drying area, qualification / re-qualification activities in Parenteral manufacturing Area (Block-E).
  9. Up-keeping the cGMP document of area and equipment log books.
  10. Any other job assigned by Department head.

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