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Manufacturing Specialist 1, Materials

Job Location:

Holly Springs, MS - USA

Monthly Salary: Not provided by the employer

Posted: 17 July 2026 (30+ days ago)

Application Deadline: 14 October 2026

Vacancies: 1 Vacancy

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Job Summary

Position Overview

Help build and sustain reliable compliant manufacturing at a worldclass 24/7 biomanufacturing site. As a Manufacturing Specialist I Materials you will be a key driver of operational readiness daily production excellence and continuous improvement. This role supports a roundtheclock operation and may require flexibility with working hours and shift rotation.

Company Overview

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs North Carolina. By end of 2025 well open North Americas largest end-to-end CDMO biopharmaceutical manufacturing facility offering drug substance production fill-finish and packaging under one roof.

Were 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 were proud to cultivate a culture that will fuel your purpose energy and drivewhat we call Genki. Ready to shape the future of medicine Lets transform healthcare together!

Holly Springs North Carolina combines small-town warmth with proximity to Raleighs thriving tech scene making it the perfect blend of community and opportunity.

Fujifilm is globally headquartered in Tokyo with over 70000 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: Description

Why this role matters

You will blend handson support with strong documentation planning and problemsolving to keep production running smoothly and safely. Your work will directly impact product quality schedule adherence and the success of technology transfers and inspections.

During project phase:

Support operational readiness initiatives as well as site commissioning and qualification efforts.

Support troubleshooting acting as a process subject matter expert for assigned area(s).
Coordinate batch planning including process template creation import and management of preventive maintenance activities.
Maintain accurate current documentation; drive timely updates to records and implement redlines and process improvements.
Coordinate nonbatch activities including changeovers preventive maintenance and column packing.
Assist with inventory management and support use of enterprise systems (e.g. SAP) for effective manufacturing operations.
Support technology transfer within the manufacturing domain.
Ensure compliance with procedures and safety requirements in the manufacturing environment.
Manage perform initiate or support change management records investigations corrective and preventive actions and continuous improvement activities.
Identify and drive improvement projects in drug substance manufacturing.
Assist and support internal and external inspections and audits to maintain compliance.
Perform other duties as assigned to meet production and quality objectives.

24/7 operational facility; flexibility with working hours and shift rotation is required.

Minimum education and experience

High School Diploma/GED and 10 years of related experience; OR
Associates degree preferably in life sciences or engineering with 8 years of direct experience; OR
Bachelors degree preferably in life sciences or engineering with 6 years of direct experience; OR
Equivalent military experience/training.

Preferred qualifications

Strong current Good Manufacturing Practice (cGMP) manufacturing operations experience.
Solid understanding of operations sequence and cadence of activities.
Prior experience updating and creating manufacturing documents according to schedule.

Training and certifications

Preferred: BioWorks or BTEC Capstone cGMP coursework.

What helps you succeed here

Strong verbal and written communication skills.
Excellent time management and the ability to prioritize in a fastpaced environment.
Adaptabilityable to pivot and adjust plans as priorities shift.
Critical thinking and superior problemsolving skills.
A teamfirst mindset with the ability to work effectively in a global crossfunctional environment and build strong relationships.

Ready to make an impact in a highgrowth highstandards manufacturing environment Apply today and help us deliver lifechanging medicines with quality and speed.

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 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 committedto 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 ().

Required Experience:

IC

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About Company

Fujifilm

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