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Manufacturing Associate 4 (Downstream) Day Shift (2-2-3)

Job Location:

Holly Springs, MS - USA

Monthly Salary: Not provided by the employer

Posted: 2 July 2026 (30+ days ago)

Application Deadline: 17 October 2026

Vacancies: 1 Vacancy

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Job Summary

Position Overview

Help us deliver reliable compliant biomanufacturing. We are hiring a Manufacturing Associate 4 to lead and execute manufacturing processing activities in a cGMP this senior role you will support both project-phase readiness (procedures process transfer testing/commissioning) and steady-state operations in a 24/7 facilityhelping ensure safe consistent and efficient production of drug substance. You will also assist with daily scheduling and materials oversight for the manufacturing team.

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

What Youll Do

Contribute to operational readiness for bulk drug substance manufacturing during the project phase.
Support procedure review/creation and development or transfer of manufacturing business processes.
Provide testing and commissioning support for equipment/systems; travel up to 025% (domestic or international) may be required during the project phase.
Lead execute and document manufacturing processing steps and/or support activities; perform process monitoring and control per cGMP standards.
Perform in-process testing (e.g. pH conductivity visual inspection).
Execute validation protocols according to cGMP Standard Operating Procedures (SOPs).
Maintain required training and qualifications for all assigned manufacturing activities.
Assist and/or lead cycle counts and manage materials for the assigned manufacturing area.
Support and/or assist senior-level associates or the supervisor with scheduling daily activities on the manufacturing floor as needed.
Work assigned shifts in a 24/7 operation including weekends and potential nights.
Perform other duties as assigned.

Minimum Qualifications

High School Diploma or GED and 6 years of experience in life sciences manufacturing; or
Associate degree and 4 years of experience in life sciences manufacturing; or
BA/BS and 2 years of experience in life sciences manufacturing; or
Equivalent military training/experience.
Advanced understanding of manufacturing run cadence and order of shift activities.
Knowledge of cGMPs safety and operational procedures.
High level of knowledge and expertise operating specific production equipment.
Strong troubleshooting ability; ability to follow technical instructions and document accurately.
Strong verbal and written communication; effective team collaboration skills.
Strong time management; ability to adapt in a fast-paced changing environment and pivot as needed.
Willingness to work shifts (including weekends/nights); travel up to 025% during the project phase as needed.

Preferred Qualifications

BioWorks or BTEC Capstone cGMP coursework.

Physical Requirements

The physical demands described here are representative of those that may be required to successfully perform essential job functions in a manufacturing environment. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Requirements may include:

Standing and/or sitting for prolonged periods.
Performing repetitive motions involving wrists hands and fingers.
Working in proximity to production equipment and utilities.
Lifting or moving materials as required by task-specific SOPs and safety guidelines.

To all agencies: Please no phone calls or emails to any employee about this requisition. All resumes submitted by search firms/employment agencies to any employee via email the internet or in any form and/or method will be deemed the sole property of the company unless such search firms/employment agencies were engaged for this requisition and a valid agreement is in the event a candidate who was submitted outside of the approved 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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