GMP Manufacturing Quality Associate; Temp; Onsite
Listed on 2026-10-06
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Quality Assurance - QA/QC
Production QC/QA, Regulatory Compliance Specialist -
Manufacturing / Production
Production QC/QA, Pharmaceutical Manufacturing, Regulatory Compliance Specialist
Kedrion Biopharma Inc. is seeking a Manufacturing Quality Associate for a day shift on a temporary basis in Melville, NY.
The role sits on the production floor in a GMP-regulated environment, supporting quality oversight, batch review, and documentation to ensure compliance with procedures and regulatory standards. You will collaborate with Quality, Operations, and Engineering to monitor activities, perform inspections, and initiate non-conformance reports while contributing to continuous
We have an opening for a GMP Manufacturing Quality Associate (Temp) - Onsite in Melville, NY, United States within Bio & Pharmacology & Health, Engineering.
The following opening is for a GMP Manufacturing Quality Associate (Temp) - Onsite with Kedrion Biopharma GmbH.
Our organisation is growing, and we are hiring a GMP Manufacturing Quality Associate (Temp) - Onsite in Melville, NY, United States.
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