Life Science Jobs at Fujifilm Biotechnologies
FUJIFILM Biotechnologies is hiring Manufacturing Associates – Biologics (Day Shift) for multiple openings at its state-of-the-art facility in Holly Springs, North Carolina. This role offers a unique opportunity to be part of a cutting-edge biopharmaceutical manufacturing organization supporting drug substance and drug product production. Candidates getting hired for the Manufacturing Associate position at Fujifilm careers will contribute to operational readiness, commissioning, and cGMP-compliant manufacturing in a 24/7 production environment.
Job Details:
- Job Title: Manufacturing Associate – Biologics
- Shift: Day Shift (Approx. 6:00 AM – 6:00 PM)
- Schedule: 12-hour shifts, 2-2-3 rotation
- Location: Holly Springs, North Carolina, United States
- Employment Type: Full-Time
- Industry: Biopharmaceutical Manufacturing (CDMO)
- Openings: Multiple roles across Manufacturing Associate
About the Company:
FUJIFILM Biotechnologies is building North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility in Holly Springs, NC. By the end of 2025, the site will offer integrated drug substance production, fill-finish, and packaging under one roof. Globally headquartered in Tokyo, FUJIFILM employs over 70,000 people worldwide across healthcare, electronics, imaging, and business innovation. Guided by its purpose of “giving our world more smiles,” FUJIFILM careers fosters a mission-driven culture known as Genki, empowering employees to shape the future of medicine.
Educational Requirements for the Manufacturing Associate:
Requirements vary by Manufacturing Associate level:
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Manufacturing Associate 2
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High School Diploma or GED with 2 years of life sciences manufacturing experience, or
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Associate’s Degree in Life Sciences, or
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Equivalent military training/experience
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Manufacturing Associate 3
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High School Diploma or GED with 4 years of experience, or
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Associate’s Degree with 2 years of experience, or
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BA/BS in Life Sciences, or
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Equivalent military experience
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Key Responsibilities of the Manufacturing Associate:
- Participate in testing activities such as FAT and PQ
- Support documentation preparation, including SOPs and Work Instructions
- Contribute to operational readiness for weigh & dispense, drug substance, and drug product manufacturing
- Support commissioning, qualification, and process transfer activities
- Execute and document manufacturing processing steps in compliance with cGMP
- Perform functional area operations, monitoring, and process control
- Execute validation protocols following SOPs
- Maintain GMP compliance and personal training records
- Serve as a trainer for coworkers when qualified
- Support scheduling and daily operations as needed
- Perform shift work, including weekends and potential nights
- Complete additional duties as assigned
Skills Required for the Manufacturing Associate Role:
- Experience in life sciences or biopharmaceutical manufacturing
- Strong understanding of cGMP regulations
- Ability to execute and document manufacturing processes accurately
- Attention to detail and a compliance-driven mindset
- Ability to work in a 24/7 shift-based manufacturing environment
- Strong teamwork and communication skills
- Willingness to support operational readiness and startup activities
Benefits of the Life Science Jobs:
- Opportunity to work at a brand-new, world-class biomanufacturing facility
- Long-term career growth within a global biopharmaceutical organization
- Exposure to end-to-end CDMO manufacturing operations
- Collaborative, mission-driven work culture focused on innovation and purpose
- Competitive compensation and comprehensive benefits package
- Inclusive workplace with strong commitment to diversity, equity, and inclusion
