Job Description

Position Overview:

The Scientist 1, QC Microbiology, DP & RM, effectively and efficiently manages complex or difficult tasks with expertise within the assigned disciplines. This role initially supports the commissioning activities involved in the construction of a new Biopharmaceutical manufacturing facility and laboratory. Flexibility in job roles and assignments is required.
Company Overview:

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


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What You'll Do

Performs raw material microbial assessments, identifies requirements and executes actions as part of change control process Performs high throughput, right-first time work to meet production schedules and project milestones with minimal/no supervision Implements new raw materials, including specification authoring, requesting LIMS builds, assessing changes etc.. Supports raw material life cycle management (new material assessment, specification establishment, maintenance of specifications etc.) Coordinates and is responsible for raw material data review and release for the Microbiology team Acts as subject matter experts for both raw materials and drug product manufacturing support Initiates qualification and study directed testing activities in support of Drug Product manufacturing Initiates technical writing initiatives and promotes problem-solving skills among the team Reviews and evaluates advanced lab testing results both internally and from third party laboratories Performs testing and review of QC samples Serves as point of contact to third party laboratories Authors, reviews, and edits documents and study protocols Supports intermediate investigations of OOS assays and events Ensures compliance with cGMP and participates in audits and inspections Provides OOS investigational support, as needed Supports laboratory management and mentors' others on the team, as needed Leads LEAN lab and six sigma principles and applies them to laboratory processes Acts as project leader for projects in the lab and department Performs other duties, as assigned

Minimum Requirements:

Bachelor's degree in chemistry, Biochemistry, Microbiology or other
relevant scientific discipline with 6+ years' experience OR

Master's degree in chemistry, Biochemistry, Microbiology or other
relevant scientific discipline with 3+ years' experience OR

PhD with 1+ years of applicable industry experience 1-3 years of experience working in a regulated GMP environment Expert understanding of GMP, GLP, GDP requirements Experience and proficient knowledge in Microbiology theory Experience and proficient knowledge of Microbiology testing and
laboratory experience, specific to both Drug product manufacturing


support and raw materials testing.


LIMS experience Experience with document control including writing and
editing technical documents and presentations

Preferred Requirements:

Knowledge in Microbiology theory Knowledge of Microbiology testing and laboratory experience, specific to both Drug product manufacturing support and raw materials testing

Physical and Work Environment Requirements:

Ability to discern audible cues.
Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color.
Ability to stand for prolonged periods of time up to 60 minutes.
Ability to sit for prolonged periods of time up to 60 minutes.
Ability to conduct activities using repetitive motions that include wrists, hands and/or fingers.
Ability to conduct work that includes moving objects up to 10 pounds.
Ability to bend, push or pull, reach to retrieve materials from 18" to 60" in height, and use twisting motions.
Will work in warm/cold environments (5 C)
Will work in small and/or enclosed spaces.

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.




EEO Information:

Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.
ADA Information:

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).