Associate Quality Control - Nights

Role: Associate Quality Control (Night Shift) supporting routine testing in a biopharma manufacturing environment at Amgen Rhode Island. Responsibilities include executing laboratory tests on samples from manufacturing, raw materials, environmental monitoring, and utilities; ensuring compliance with cGMP, safety, and regulatory standards; generating accurate documentation; operating lab equipment; reviewing assays and records; supporting troubleshooting, deviations, and continuous improvement initiatives. Requirements: High school diploma/GED with 2 years of QC experience, or Associate’s degree with 6 months of QC experience, or Bachelor’s degree. Preferred skills include experience with analytical/biological testing, QC systems, technical writing, and operational excellence. The role emphasizes attention to detail, teamwork, and adherence to regulatory standards within a highly regulated environment. High-value specifics: biopharma manufacturing, microbiology, biochemistry, environmental monitoring, cGMP compliance, night shift, part of the Quality Control team at a biologics manufacturing site. Collaboration: reports to management, supports cross-functional teams. Work setup: night shift at Rhode Island site, no travel specified.