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Amgen Logo Amgen · Manufacturing

Manufacturing Process Technician

United States, Holly Springs 57623.00 - 68426.00 USD / Year · Job Posted February 08, 2026
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Job Description

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleXBatch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleXBatch 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. In this vital role you will be a Mfg. Process Technician in the Upstream manufacturing organization at Amgen North Carolina (ANC). The essential position, which supports our critical 24/7 manufacturing operations, works a 12-hour 2-2-3 schedule from 5:45am to 6:15pm. Mfg. Process Technician will complete operations on the floor in the Services area and are responsible for the manufacturing of cGMP (current Good Manufacturing Practices) drug substances.

Job Responsibility

  • Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance
  • Documents accurately tasks performed and/or verified
  • Ensure proper gowning and aseptic techniques are always followed
  • Perform hands-on operation including set-up, cleaning, sanitization, monitoring of equipment in assigned area
  • Buffer and Media preparation and transfer
  • Complete washroom activities: cleaning equipment, small to large scale, used in production activities
  • Run and monitor critical processes per assigned procedures
  • Perform documentation for assigned function (i.e., equipment logs, EBRs)
  • Maintain an organized, clean, and workable space.

Requirements

  • High school diploma / GED + 1 year of manufacturing and/or other regulated experience
  • Associate’s degree
  • Completion of NCBioWorks Certificate Program
  • Experience in a regulated industry such as biotechnology or pharmaceutical
  • Basic understanding of GMP principles
  • Strong verbal and written communication skills
  • Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems
  • Ability to perform assignments with a high degree of focus/attention to detail.

Nice to have

  • Completion of NCBioWorks Certificate Program
  • Experience in a regulated industry such as biotechnology or pharmaceutical
  • Basic understanding of GMP principles
  • Strong verbal and written communication skills
  • Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems
  • Ability to perform assignments with a high degree of focus/attention to detail.

What we offer

  • Competitive and comprehensive Total Rewards Plans
  • Competitive benefits
  • Collaborative culture
  • Support for professional and personal growth and well-being.
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