Holly Springs, NC, US
1 day ago
Manufacturing Associate 2 - Upstream (Day Shift)
Welcome page Returning Candidate? Log back in! Manufacturing Associate 2 - Upstream (Day Shift) Job Locations US-NC-Holly Springs Posted Date 22 hours ago(11/12/2025 10:53 AM) Requisition ID 2025-36145 Category Manufacturing Company (Portal Searching) FUJIFILM Biotechnologies Position Overview

The role as Manufacturing Associate 2 will execute and document manufacturing processing activities within a cGMP environment. This manufacturing facility will be 24/7 operational and the role may require to be flexible 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, 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

Job Description

What You’ll Do

 

During Project Phase:

Contribute to the preparation for operational readiness related to bulk drug substance manufacturingPossible assignments include: Supporting projects related to - Procedure review and/or creation, development or transfer of manufacturing business processes, testing and commissioning supportTravel up to 0-25% (international or domestic) may be required

 

In Operations:

Execute and document manufacturing processing steps and/or manufacturing support activities; process monitoring and controlPerform in-process testing (pH, conductivity, visual inspection)Execute validation protocols according to cGMP Standard Operating Procedures (SOPs)

This role requires shift work (weekend and potential for nights)

Maintain training to perform all required activities  Perform all other duties as assigned

Who You Are

 

You have knowledge of the operations of support process equipment. You have an understanding of a cGMP environment, safety and operational procedures. You have the ability to perform operations and document them accurately. You have the ability to follow technical instructions and document them. You have strong verbal and written communication skills. You have the ability to work closely and effectively in a team environment. You have the ability to adapt in a fast-paced changing environment.

 

Basic Requirements

High School Diploma or GED2 years of related experience

Preferred Requirements

Associate’s Degree, preferably in Life Sciences or similar2 Years of direct experience in a cGMP manufacturing environmentQualified on a support area (i.e. Formulation Buffer Prep, Media Prep or DSM Buffer Prep)BioWorks or BTEC Capstone cGMP coursework preferred

WORKING CONDITIONS & PHYSICAL REQUIREMENTS

Be exposed to an environment that may necessitate respiratory protectionBe exposed to noisy environmentsHave a normal range of visionClimb ladders and stairs of various heightsExperience prolonged sitting, standing, walking, bending, stooping and stretching throughout the shift, up to 12 hoursUse hand-eye coordination and manual dexterity sufficient to operate a computer keyboard, telephone, calculator, and other office equipment is requiredMay be required to lift up to 50 pounds on occasion

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).

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