Manufacturing Associate Hiring Event (October 24th)

Fujifilm•Holly Springs, NC
•Onsite

About The Position

This role is part of an invite-only hiring event. Candidates will be screened prior to scheduling. If selected, you’ll be asked to provide your availability for interviews on October 24. No walk-ins will be accepted on the day of the event. FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof. We’re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we’re proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki. Ready to shape the future of medicine? Let’s transform healthcare together! Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers

Requirements

  • Experience in manufacturing or related field; level commensurate with role (II–V)
  • Familiarity with GMP/cGMP or regulated production environments preferred
  • Ability to follow SOPs, document accurately, and meet throughput targets
  • Strong attention to detail, teamwork, and communication skills
  • Willingness to work [shift/rotating/weekends], as needed
  • Physical requirements: ability to stand for extended periods and lift up to [X] lbs

Responsibilities

  • Support manufacturing operations in a regulated environment to meet safety, quality, and production goals
  • Execute standard operating procedures (SOPs) and batch records accurately
  • Operate, monitor, and troubleshoot production equipment; perform in-process checks
  • Maintain cGMP/5S compliance, documentation, and area readiness
  • Collaborate with cross-functional teams (Quality, Engineering, Planning)
  • Contribute to continuous improvement, root cause analysis, and safety initiatives
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