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.

Associate IS Bus Sys Analyst

What you will do

Let’s do this. Let’s change the world. In this vital role you will we are seeking a highly skilled Associate Systems Analyst to join our Quality Control Product team. You will be responsible for validation, and maintenance of software applications and solutions that meet business needs and ensuring the availability and performance of critical systems and applications. A significant part of this role includes ensuring that QC applications such as Sample Manager LIMS, ELN, and Empower CDS are implemented, configured, and maintained in compliance with Computer System Validation (CSV) / Computer Software Assurance (CSA) expectations. You will work closely with product managers, business SMEs, validation teams, and technical partners to deliver high‑quality, compliant, and scalable QC solutions, while ensuring system availability, audit readiness, and strong data integrity controls.

Roles & Responsibilities:

• Maintain existing code and configuration: Support and maintain Quality Control applications
• CSV/CSA Support: Assist in developing and executing validation deliverables (risk assessments, test scripts, traceability matrices etc) aligned with GxP, 21 CFR Part 11, data integrity, and CSA principles.
• Documentation: Produce clear documentation for functional specs, configuration updates, validation evidence, and operational procedures to maintain system audit readiness.
• Collaborative Design: Work closely with team members and collaborators to understand project requirements and translate them into functional technical designs.
• Testing & Debugging: Contribute to unit, integration, and validation (IQ/OQ/PQ) testing activities. Troubleshoot issues in QC systems and work with validation teams to maintain compliance.
• Application Support: Perform system administration tasks - periodic reviews, access management, incident resolution, audit preparation, and change‑control documentation.
• Continuous Learning: Stay up-to-date with the newest technologies and standard methodologies, with a focus on expanding knowledge in cloud services, automation, and secure software development.