Pharma Finishing Supervisor — cGMP, Fast-Paced Ops
Listed on 2026-10-17
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Manufacturing / Production
Pharmaceutical Manufacturing, Production Manager, Production Associate / Production Line, Validation Engineer -
Pharmaceutical
Pharmaceutical Manufacturing, Validation Engineer
Grand River Aseptic Manufacturing Inc. (GRAM) seeks a Finishing Supervisor to oversee multi-finishing operations of parenteral liquid drug products, ensuring compliance with cGMPs, SOPs, batch records, and labor and material standards while meeting the forecasted production schedule.
The role requires 2–5 years in a pharmaceutical or FDA-regulated environment, GMP knowledge, and ability to supervise both manual and automated processes.
The following opening is for a Pharma Finishing Supervisor — cGMP, Fast-Paced Ops with Grand River Aseptic Manufacturing Inc.
We are currently recruiting a Pharma Finishing Supervisor — cGMP, Fast-Paced Ops for our team in Grand Rapids, MI, United States.
This is a genuine role to take on the Pharma Finishing Supervisor — cGMP, Fast-Paced Ops role at Grand River Aseptic Manufacturing Inc.
As a Pharma Finishing Supervisor — cGMP, Fast-Paced Ops, you will play an important part at Grand River Aseptic Manufacturing Inc. in Grand Rapids, MI, United States.
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