Manufacturing Associate, Bulk Drug Substance Upstream - Days

Role: Manufacturing Associate in Amgen's cGMP upstream drug substance manufacturing at the new FleX Batch facility, supporting flexible, industry 4.0-enabled operations. Responsibilities: perform hands-on upstream processing, equipment setup, cleaning, monitoring, in-process sampling, and documentation; ensure compliance with cGMP standards; collaborate with cross-functional teams including QA/QC, engineering, and regulatory. Requirements: High School diploma + 2 years manufacturing/regulatory experience, Associate’s degree + 6 months experience, or Bachelor’s degree; proficiency in electronic batch records and basic process understanding preferred. High-Value: biologics manufacturing, cGMP compliance, upstream drug substance production, industry 4.0 technologies, regulated environment experience, cross-functional team collaboration. WorkSetup: rotating 12-hour day shifts, on-site in North Carolina, with potential for remote work arrangements.