Associate Manufacturing

Career Category

Manufacturing

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.

Let’s do this. Let’s change the world. In this vital role you will support the Formulation and Filling operations according to Standard Operating Procedures (SOPs). Will perform and supervise critical processes, execute routine protocols, and regularly draft and revise documents such as Manufacturing Procedures and SOPs. Perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams.

May identify, recommend, and implement improvements related to routine functions in a Non-Standard Shift environment. Multiple Positions Available.

• Conduct routine sanitization of equipment and manufacturing areas in compliance with established procedures and regulatory standards.
• Support validation activities, documentation review (e.g., batch records, audits), and basic troubleshooting.
• Identify and recommend process improvements; collaborate with engineers, mechanics, or leads for complex issues.
• Monitor equipment, work spaces, and process outputs to confirm they meet safety, quality, and performance standards.
• Follow Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), and safety protocols consistently—using reader-doer or similar methods when applicable.
• Use electronic systems such as SAP, Symphony, SCADA, or batch record platforms (training provided) to record activities, track materials, and verify production data accurately.
• Complete documentation in a timely, compliant manner, applying Good Documentation Practices (GDP) to ensure traceability and readiness for inspections or audits.
• Stay informed by reviewing SOPs regularly and asking questions when clarity is needed—supporting safe and accurate execution of tasks.
• Detect and respond to equipment or process deviations early, following SOPs and escalating issues to leads or support teams when appropriate.
• Work collaboratively with peers, leads, and trainers to meet expectations, solve problems, and foster a respectful, team-oriented work culture.
• Adapt to changing priorities and offer support to the team during downtime or as directed by your lead or supervisor to maintain operational flow.
• Participate in daily team meetings and use communication tools and production tracking systems to align your work with real-time production needs.
• Demonstrate commitment, flexibility, and attention to detail to complete tasks efficiently—especially within a dynamic, round-the-clock production environment.

We are all different, yet we all use our unique contributions to serve patients. The Associate Manufacturing professional we seek is an individual contributor with these qualifications:

• High school/GED and 2 years of manufacturing work experience

• Associate’s degree and 6 months of manufacturing work experience

• Bachelor's Degree

• Experience with Drug Product formulation and/or aseptic filling manufacturing process
• Expertise in filling line technologies, including aseptic filling equipment, isolator technology, air handling systems, and visual…