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.

BASIC QUALIFICATIONS:

Bachelor’s Degree
OR
Associate’s + 6 months Quality Control/Laboratory work
OR
High school/GED + 2 years Quality Control/Laboratory work

PREFERRED QUALIFICATIONS:

• Educational background in Biochemistry or Life Sciences
• Laboratory experience in a GMP environment within the Pharmaceutical and/or Biotech industry
• Ability to adhere to regulatory requirements, written procedures, and safety guidelines, following GMP regulations
• Ability to organize work, handle multiple priorities and meet deadlines
• Good written and oral communication skills including technical writing capabilities
• Good presentation skills
• Detail oriented
• Flexible and adaptable to changing priorities and requirements
• Bilingual Fluent in both Spanish and English languages
• Ability to relate day-to-day work to business priorities
• Availability to work non-standard shift including 3rd shift

WHAT YOU WILL DO

Let’s do this. Let’s change the world! In this vital role you will be responsible for one or more of the following activities: analytical testing, method development, routine sample testing, and data management. This role is a key contributor within the Quality Control department and supports non-standard shift operations, which may include first, second, third, and/or weekend shifts.

SPECIFIC RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO:

• Conduct routine laboratory testing using techniques such as SDS Page, IEF, Capillary Electrophoresis and Elisa in accordance with SOPs, compendia, and analytical methods.
• Operate laboratory equipment and confirm materials, reagents, and consumables are within expiry prior to use.
• Evaluate test results accurately and identify unexpected or out-of-specification outcomes.
• Capture and document test data using laboratory systems (e.g., LIMS, Empower, LMES) in accordance with Good Documentation Practices.
• Initiate troubleshooting or root cause analysis in alignment with SOPs and bring up unresolved issues or deviations to the manager promptly.
• Collect, organize, and track samples following SOPs and internal timelines.
• Monitor tracking tools (e.g., Smartsheet, sample progress reports) to guide task completion and sample status.
• Ensure sample testing and documentation meet established due dates and business priorities.
• Replenish and manage laboratory inventory and prepare materials during downtime for upcoming tests.
• Follow all lab safety, cGMP, and quality standards throughout testing activities.
• Complete all assigned training on time and stay current with SOPs and analytical methods.