Entry-Level: Manufacturing Associate 1 and 2/Night Shift
Listed on 2026-10-05
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Manufacturing / Production
Pharmaceutical Manufacturing, Production Associate / Production Line, Manufacturing & Industrial Operations, Production QC/QA
Position Overview
Help deliver reliable, compliant biomanufacturing. We are hiring a Manufacturing Associate 1 and 2 to assist with the execution and documentation of manufacturing processing activities in a cGMP environment. The role supports project-phase readiness and steady-state operations in a 24/7 facility—helping maintain safe, consistent, and efficient production. Flexibility with working hours and shift rotations is required.
Company OverviewFUJIFILM 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:
Job DescriptionWhat You’ll Do
- Support operational-readiness activities for biopharmaceutical manufacturing.
- Assist with procedure review, document preparation, testing, commissioning, and equipment-readiness activities.
- Execute and document assigned manufacturing processing and support activities according to SOPs and cGMP requirements.
- Perform process monitoring and in-process testing, such as pH, conductivity, and visual inspections.
- Follow technical instructions and accurately document completed work.
- Complete and maintain all required training and qualifications.
- Work collaboratively with experienced associates, technical staff, and supervisors.
- Follow all safety, quality, and operational procedures.
- Perform other duties as assigned.
Manufacturing Associate 1
Minimum Qualifications:
- High School Diploma or GED
- 0–2 years of work experience.
- Flexibility to work shifts in a 24/7 environment.
- Basic knowledge of assigned process equipment
- Basic understanding of cGMPs, safety, and operational procedures
- Ability to follow technical instructions and document accurately using good documentation practices.
- Ability to assist with operations, learn quickly, ask questions, and work effectively in a team.
- Willingness to work shifts (including weekends/nights).
Manufacturing Associate 1
Preferred Qualifications:
- Associate degree, preferably with 1–2 years of direct experience in a cGMP manufacturing environment.
- Bio Works or BTEC Capstone cGMP coursework (preferred if no prior GMP experience).
Manufacturing Associate 2 Miniumum Qualifications
- High School Diploma or GED AND 2 years of related experience (or equivalent combination of education and experience).
- 2+ years of direct experience in a cGMP manufacturing environment.
- Knowledge of support process equipment and understanding of cGMPs, safety, and operational procedures.
- Ability to perform operations and document them accurately; ability to follow technical instructions.
- Strong verbal and written communication; ability to work effectively in a team.
- Ability to adapt in a fast-paced, changing environment.
- Willingness to work shifts (including weekends/nights).
Manufacturing Associate 2
Preferred Qualifications:
- Associate degree in Life Sciences or a related field.
- Qualified in a support…
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