Manufacturing Associate - Bulk Drug Substance Manufacturing Services - Days

Role: Manufacturing Associate supporting bulk drug substance manufacturing at Amgen's North Carolina facility expansion, focusing on operational readiness, media/buffer preparation, equipment setup, and routine GMP manufacturing activities. Responsibilities: perform weigh and dispense of raw materials, support equipment sanitation, execute process operations, ensure compliance with cGMP, document activities, and collaborate with cross-functional teams during startup and steady-state production. Requirements: High School/GED + 2 years regulated environment experience, or Associate’s Degree + 6 months, or Bachelor’s Degree; strong communication skills; proficiency in Microsoft Office; knowledge of electronic batch records and manufacturing systems preferred. High-value: biologics manufacturing, cGMP compliance, media/buffer prep, facility startup, 24/7 shift work, cross-functional collaboration during production ramp-up. Work setup: on-site in North Carolina, with shift flexibility during startup and steady-state operations. Occasional non-standard hours and overtime required.