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Manufacturing Associate 3, Filling

Job Location:

Holly Springs, MS - USA

Monthly Salary: Not provided by the employer

Posted: 30 August 2026 (18 days ago)

Application Deadline: 27 November 2026

Vacancies: 1 Vacancy

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Job Summary

Position Overview

Help deliver safe high-quality medicines at scale. As a Manufacturing Associate 3 Drug Product youll play a hands-on role in component/parts preparation thawing and formulation sterile filling and visual inspectionsupporting a 24/7 operation that keeps patients at the center.

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

We are a collaborative Drug Product manufacturing team committed to operational excellence safety and cGMP compliance.
Youll help shape processes train new colleagues and support equipment qualification and startup activities for our DPFG facility.
Our environment values clear communication teamwork and continuous improvementso you can contribute learn and grow.

Minimum qualifications (one of the following is required):

High School Diploma or GED with 4 years of direct experience in a cGMP manufacturing environment; OR
Associates Degree with 2 years of direct experience in a cGMP manufacturing environment; OR
Bachelors Degree (preferably Life Sciences or Engineering); OR
Equivalent military training or experience

Preferred qualifications:

Qualified experience on unit operations such as Parts Washer Autoclave Operation Compounding/Formulation Filling with Isolator Technology or Manual/Automated Visual Inspection
BioWorks or BTEC Capstone cGMP coursework

What helps you succeed:

Ability to assist in troubleshooting and apply sound judgment on assignments
Strong verbal and written communication skills
Knowledge of production equipment operations within your unit operation(s)
Basic understanding of manufacturing run cadence and order of shift activities
Knowledge of cGMP safety and operational procedures
Ability to work effectively in a team environment
Flexibility for shift rotation and weekend/night work in a 24/7 facility

Responsibilities

Lead execute and document manufacturing processing steps and/or support activities including process monitoring and control
Perform in-process testing (e.g. pH conductivity visual inspection) with accuracy and attention to detail
Execute validation protocols in alignment with cGMP Standard Operating Procedures (SOPs)
Maintain training qualifications to perform all required manufacturing activities
Perform operations across Drug Product unit operations including:
- Parts Washer and Autoclave
- Compounding/Formulation
- Sterile Filling (including isolator technology)
- Manual and/or Automated Visual Inspection
Assist and/or lead cycle counts; manage materials for assigned manufacturing areas
Assist the lead with daily manufacturing tasks and coordinate daily shift activities as needed
Support projects that improve Drug Product manufacturing processes including training of new colleagues
Maintain compliance of cGMP documents and assist in equipment qualification and DPFG facility startup activities
Follow safe work practices and escalate issues promptly to maintain product quality and compliance
This role may require shift work (weekends and potential nights) and other duties as assigned

Competitive pay with shift differentials where applicable
Comprehensive health coverage (medical dental vision)
Paid time off holidays and sick leave
Retirement savings plan with company contribution
Training and development opportunities including cGMP upskilling and mentorship
Inclusive team-centered culture focused on safety quality and continuous improvement
Employee assistance and well-being resources
Opportunities to contribute to startup and optimization initiatives in a modern DP facility

Work environment and physical requirements (role-specific)

May require respiratory and hearing protection; ability to discern audible cues and perform tasks requiring 20/20 corrected vision (including color)
Ability to ascend/descend ladders; perform repetitive motions with wrists/hands/fingers
Ability to operate machinery/power tools and as required motor vehicles or Powered Industrial Trucks
Ability to lift/move up to 33 lbs; bend push/pull and reach between 18 and 60 in height
Comfortable working at heights greater than 4 feet
Prolonged standing and sitting may be required depending on shift activities

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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