SUSun Pharma
Senior Manager Production Injectables
Kolkata ₹5-11 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
- He is authorize to sign ( as a doer, reviewer & Approver ):
- Parenteral GMP documents
- Breakdown memo perform impact analysis
- Equipment and Area cleaning/sanitization logs
- He is responsible for overall QMS activity.
- Involved in the equipment Qualification / Re-Qualification activity in parenteral Manufacturing area (Block-E).
- He is responsible for activities related to parenteral Manufacturing area (Block-E).
- 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).
- Up-keeping the cGMP document of area and equipment log books.
- Any other job assigned by Department head.
