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Manufacturing Associate 3, Visual Inspection (Second Shift 3pm to 1130pm)

Job Location:

Holly Springs, MS - USA

Monthly Salary: Not provided by the employer

Posted: 9 August 2026 (26 days ago)

Application Deadline: 20 November 2026

Vacancies: 1 Vacancy

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Job Summary

Position Overview

Do you thrive in a fast-paced highly regulated environment where precision teamwork and continuous improvement make a real difference for patients Join our Drug Product team as a Manufacturing Associate III to lead hands-on operations across formulation sterile filling and visual inspectionwhile helping stand up and optimize a state-of-the-art DP facility.

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 mission-driven biopharmaceutical manufacturer dedicated to reliably supplying high-quality therapies. Our culture is inclusive safety-focused and rooted in collaboration and learning. We invest in our people value diverse perspectives and empower team members to grow their careers while making meaningful impact for patients.

Responsibilities

Lead execute and document manufacturing processing steps and manufacturing support activities including process monitoring and control.
Perform in-process testing including:
pH conductivity and visual inspection.
Execute validation protocols in accordance with cGMP Standard Operating Procedures (SOPs).
Maintain current training to perform all assigned manufacturing activities.
Assist and/or lead cycle counts; manage materials for the assigned manufacturing functional area.
Perform operations across Drug Product areas such as:
Parts washing and preparation.
Autoclave operation.
Thawing and compounding/formulation of drug substance.
Sterile filling (including isolator technology).
Manual and/or automated visual inspection.
Support projects that improve Drug Product manufacturing processes including:
Training of new colleagues.
Maintaining cGMP documentation.
Assisting in equipment qualification and all aspects of DPFG facility startup.
Assist the lead with manufacturing tasks and help coordinate daily shift activities to ensure smooth safe operations.
Work a shift schedule to support a 24/7 operation (weekends and potential nights may be required).
Perform other duties as assigned.

Qualifications Minimum:

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 in Life Sciences or Engineering); or
Equivalent military training or experience.
Qualified experience on at least one unit operation such as:
Parts washer autoclave operation compounding/formulation filling with isolator technology or manual/automated visual inspection.

Qualifications Preferred:

BioWorks or BTEC Capstone cGMP coursework.

Skills and traits for success:

Ability to assist in troubleshooting and recommend solutions.
Strong verbal and written communication skills.
Knowledge of production equipment in your assigned unit operation(s).
Basic understanding of manufacturing run cadence and order of shift activities.
Working knowledge of cGMP safety and operational procedures.
Ability to work effectively in a team environment and exercise sound judgment and initiative.

Work environment and physical requirements:

May require respiratory protection; may work in mechanical/production spaces requiring hearing protection and enrollment in a hearing conservation program.
May operate a motor vehicle or Powered Industrial Truck (PIT).
Ability to discern audible cues and perform tasks with 20/20 corrected vision including color differentiation.
Ability to ascend/descend ladders scaffolding and ramps; work at heights greater than 4 feet.
Ability to stand and sit for prolonged periods; perform repetitive motions with wrists hands and/or fingers.
Ability to operate machinery and/or power tools.
Ability to move objects up to 33 lbs; bend push/pull and reach from 18 to 60 with twisting motions.
No routine work in outdoor elements small/enclosed spaces or extreme temperatures.

Inclusive team-first culture with strong emphasis on safety quality and continuous improvement.
Hands-on experience across key Drug Product unit operations in a modern GMP facility (formulation filling with isolator technology and visual inspection).
Opportunities to mentor peers and support new-hire training as the site scales.
Professional growth and learning support including cGMP and technical training; recognition of relevant coursework (e.g. BioWorks BTEC Capstone).
Competitive compensation and comprehensive benefits package with potential shift differentials for eligible schedules.
The chance to directly impact the reliable delivery of high-quality medicines to patients.

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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