Associate Quality Compliance

Role: Controlled Documentation Associate supporting Amgen’s R&D Quality Management System by executing and maintaining controlled document workflows, ensuring compliance with global standards and GCP regulations. Responsibilities: manage document creation, revision, obsoletion, perform impact analysis, conduct quality checks, and support inspection readiness activities. Collaborates across functions to facilitate document approval, track workflows, and support audits. Requirements: high school/GED + 2 years, Associate’s + 6 months, or Bachelor’s degree; strong attention to detail; experience with document control tools; excellent communication skills; ability to prioritize tasks. Preferred: familiarity with document management systems, quality control, and GxP practices. High-Value: focus on regulated R&D environment, supporting documentation for clinical or preclinical studies. Work setup: not specified.