Engineering Project Manager

Career Category Engineering Job Description Join Amgen’s Mission of Serving Patients    At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.    Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.    Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.      Engineering Project Manager     Duties: Applies working knowledge of process equipment, material flow, and utilities commonly used in GMP manufacturing to support equipment readiness, operational transitions, and project execution. Coordinates execution activities using production schedules, project timelines, and work plans to support timely delivery of manufacturing and project milestones while maintaining full GMP compliance. Responsible for supporting manufacturing equipment readiness for use in regulated GMP environments by working in compliance with documented procedures, data integrity expectations, and applicable quality system requirements across regulated manufacturing industries. Collaborates with engineering, maintenance, and external suppliers to prepare manufacturing and processing equipment for GMP operation and confirm readiness prior to startup. Supports equipment installation, startup, and modification activities under GMP controls, ensuring work is executed in alignment with validated processes, hygiene standards, and contamination prevention requirements. Participate in commissioning, startup, and qualification activities for manufacturing equipment and utilities to verify equipment suitability for regulated production.

Master’s degree (or foreign equivalent) in Business and Science, Business Administration or a related field & 2 years of experience in the job offered or in a Manufacturing Production - related occupation. The position requires 2 years of experience in the following skills:    GMP-regulated manufacturing environments to ensure equipment readiness, site execution, and commissioning activities are performed in compliance with quality, safety, and regulatory standards necessary to support uninterrupted manufacturing operations;    Working within regulated manufacturing environments governed by GMP principles, including adherence to documented procedures, data integrity expectations, and quality system requirements applicable across regulated industries such as biopharmaceutical, biotechnology, or regulated food manufacturing;    Participation in preparing manufacturing or processing equipment for GMP use, coordinating with engineering, maintenance, and suppliers to confirm readiness before operation;    Equipment installation, startup, or modification activities under GMP controls, ensuring work is performed in a manner consistent with validated processes, hygiene requirements, and contamination prevention principles;    Participation in commissioning, startup, or qualification-related activities for manufacturing equipment or utilities, including tasks required to verify equipment suitability for regulated production;    Process equipment, material flow, and utilities knowledge used in GMP manufacturing to support installation, readiness, and operational transitions; and    Coordinating execution activities using production schedules, project