QA Specialist – Finishing Ops; cGMP Pharma Impact
Listed on 2026-10-11
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Engineering -
Pharmaceutical
Quality Engineering
Grand River Aseptic Manufacturing (GRAM) is seeking a QA Specialist I in Finishing Operations to support quality systems for parenteral drug manufacturing and testing. You will oversee terminal sterilization, visual inspection, labeling and packaging activities and release materials as part of the QA process.
The role requires 1–2 years of related experience, knowledge of QA in pharma, and proficiency with Word, Excel and Outlook.
This role, QA Specialist – Finishing Ops (cGMP Pharma Impact) at Grand River Aseptic Manufacturing Inc., could be your next move.
The advertised compensation is 65.000 - 90.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the QA Specialist – Finishing Ops (cGMP Pharma Impact) role in the description above.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).