Associate Quality Control
Amgen
October 2, 2026
Full-time
On-site
West Greenwich, RI
Operations
Role: Associate Quality Control supporting Raw Material QC testing at Amgen, focusing on wet chemistry analyses to ensure raw materials meet specifications for biopharma manufacturing. Responsibilities: operate laboratory equipment, generate accurate documentation, review assays and records, follow cGMP and safety guidelines, support investigations, and contribute to continuous improvement initiatives within the QC lab. Requirements: high school diploma/GED with 2+ years in Quality/Operations, associate’s degree with 6 months experience, or bachelor’s degree; experience with analytical testing, QC systems, and regulated environments preferred. HighValue: biopharma QC, raw materials, wet chemistry, cGMP compliance, pharmaceutical manufacturing, regulated documentation, laboratory investigations. WorkSetup: onsite at Rhode Island, Monday–Friday, shift-based; no specific travel mentioned.