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Associate Quality Control - Nights

Amgen
October 2, 2026
Full-time
On-site
West Greenwich, RI
Operations
Role: Associate Quality Control (Night Shift) at Amgen, supporting GMP analytical testing in a biopharma environment. Responsibilities: perform assays on manufacturing samples (e.g., Titer, Endotoxin, Microbiology), raw materials, environmental monitoring, and utilities; ensure compliance with GMP, GDP, safety, and regulatory standards; generate and review documentation; operate laboratory equipment; support troubleshooting, deviations, and investigations. Requirements: high school diploma/GED with 2+ years, associate’s degree with 6+ months, or bachelor’s degree; 1-3 years GMP lab experience; proficiency in analytical/biological testing per Methods/Compendia; familiarity with QC systems; strong organizational, communication, and analytical skills; understanding of biopharma processes. Preferred: experience with biopharmaceuticals, investigations, and QC procedures. HighValue: GMP analytical lab, biopharmaceuticals, night shift (Tuesday-Friday, 10 PM–8 AM), environmental and raw material testing, troubleshooting, documentation, and compliance. WorkSetup: on-site in Rhode Island.