Manufacturing Senior Associate - Single Use Systems; SUS
Listed on 2026-10-18
-
Manufacturing / Production
Quality Engineering, Manufacturing Engineer, Validation Engineer -
Engineering
Quality Engineering, Manufacturing Engineer, Process Engineer, Validation Engineer
Career Category
Manufacturing
Job Description
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you're part of something bigger, it's because you are. At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together-researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It's time for a career you can be proud of.
Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX batch facility will combine the latest in single use technologies with traditional stainless steel equipment to allow for maximum flexibility in operations The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.
ManufacturingSenior Associate
- Single Use Systems (SUS)
Live
What you will doLet's do this. Let's change the world. In this vital role you will be part of the Manufacturing Support team which is responsible for manufacturing activities such as new product introduction, new technology and equipment introduction, continuous improvement projects, supporting CAPA ownership, deviation trending, and optimization/implementation of single use technologies. The position is within the drug substance organization in Amgen North Carolina at Holly Springs.
This role is critical for Amgen North Carolina's success and key in supporting single-use (SUS) operations.
Key responsibilities include:
- Support New Product introduction and projects through SUS mapping/drawing.
- Maintain and edit SUS Standard Operating Procedures (SOP).
- Support manufacturing and quality through the SUS defect/leak triage process - perform troubleshooting on the floor, initiate investigations and bring leaks and defects to triage meetings.
- Initiate Event Notification (EN)/Supplier Investigation/Corrective Action (SICAR) records and follow process to conclusion, including collaborating with vendors on investigation.
- Maintain up-to-date EN/SICAR/Early Engagement (EE=new item) trackers and manage or lead small to medium projects.
- Provide input for ANC representative to SUS network for improvements and troubleshooting.
- Support Vendor Change Notification assessments.
- Understand single-use material capabilities and user requirements for new technologies through interaction with end users.
- Collaborate with Continuous Improvement (CI) leads to help SUS improvement projects and provide/lead use cases for continuous improvement projects. For example, improvements around tubing management, material kitting, and flow.
Win
What we expect of youWe are all different, yet we all use our unique contributions to serve patients. We are looking for a detail-oriented partner with an understanding of manufacturing operations and a passion for single-use systems, with the following qualifications:
Basic Qualifications:- High School diploma / GED and 8 years of Engineering or Operations experience
- OR
- Associate's degree and 6 years of Engineering or Operations experience
- OR
- Bachelor's degree and 2 years of Engineering or Operations experience
- OR
- Master's degree
- Experience with and understanding of Single-Use Systems.
- Experience in Drug substance GMP technical support roles, GMP manufacturing, Engineering, Process Development, or equivalent.
- Technical knowledge of drug substance processing and broad understanding of related disciplinary areas.
- Ability to successfully communicate complex technical information with internal and external colleagues of varying organizational levels in both presentation and technical writing forms.
- Ability to coach, mentor and/or cross train colleagues within core technical area.
- Team player
- Ability to support process owner team by reprioritizing or readjusting projects, tasks, or responsibilities. - Ability to drive results through leadership of cross-functional teams.
- Data analysis and/or data visualization skills
- Excellent writing skills. presentation to leadership.
- Determines work tasks and timelines self-sufficiently - ability to navigate through ambiguity and prioritize effective
- Experience in computerized systems for example, Smartsheet, Excel, Trackwise, Veeva, Visio, Lucid Chart.
- Expertise with translating business/user…
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