Distribution & Wholesale STEM OPT Jobs in North Carolina
Distribution and wholesale companies in North Carolina, including major employers in Charlotte, Raleigh, Greensboro, and the Research Triangle area, hire F-1 STEM OPT students for roles in supply chain analytics, logistics technology, and operations management. North Carolina's position as a Southeast distribution hub makes it an active state for STEM-designated sponsorship opportunities in this sector.
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Get Access To All JobsPOSITION OVERVIEW:
Help build and optimize a best-in-class LabWare LIMS v8 environment that powers Quality Control in a GMP setting. As Sr. Specialist 1, QC LIMS, you’ll configure, validate, and sustain a critical system that enables compliant, efficient testing—directly impacting product quality and patient safety.
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.”
About us
We are a collaborative Quality Control LIMS team partnering closely with Quality Control, Analytical Development, Manufacturing, IT, and Quality Assurance. Our mission is to ensure our LabWare LIMS operates in a robust, validated, and compliant state aligned with cGMP, ICH, FDA, 21 CFR Part 11, and GAMP expectations. We value curiosity, accountability, and cross-functional partnership, and we foster an inclusive environment where every voice is heard and respected.
MINIMUM QUALIFICATIONS
- Bachelor’s degree in Computer Science, Information Technology, Biology, Microbiology, Biochemistry, or a related scientific discipline with 2+ years of experience; or
- Master’s degree in the same fields with 0 years of experience
- Ability to function in a fast-paced, highly technical environment
- Demonstrated ability to work cross-functionally and build strong partnerships across levels (management, laboratory personnel, plant personnel)
- Thorough knowledge of cGMP/ICH/FDA regulations; familiarity with 21 CFR Part 11 and GAMP
- Strong verbal and written communication, technical writing, and problem-solving skills
- Understanding of pharmaceutical/biotech testing cycles or requirements
- Ability to work effectively with diverse teams
PREFERRED QUALIFICATIONS
- 1–3 years of experience in a cGMP Quality Control department or FDA-regulated industry (drugs/biologics)
- Previous experience with LabWare LIMS development or other LIMS software development
- Experience with 21 CFR Part 11 and GAMP (applied/working experience)
- TrackWise (or similar quality system) experience for at least 1 year
- Leadership aptitude
Responsibilities
- Participate in the LabWare LIMS v8 site go-live, including static data migration, configuration, validation, and cross-functional coordination to ensure a successful rollout.
- Collaborate with business subject matter experts to define and document new or revised LabWare requirements.
- Configure basic and advanced LabWare LIMS objects, including:
- Specifications, Analyses, Batch Templates, Test Lists, QC Samples
- Calculations, Format Calculations
- Templates (Stability, Sample Login, Standards, Reagents)
- Execute qualification/verification testing to support implementation of new or revised LabWare configurations.
- Maintain and, when needed, repair configuration objects within LabWare LIMS.
- Create queries to support evolving business requirements.
- Use the change management system to update configurations for specifications, analyses, and other static data in LIMS.
- Provide timely user support and troubleshooting; create new configuration templates; maintain accurate change records per version control procedures.
- Deliver LIMS training, technical support, problem reporting, and resolution for QC, QA, AD, and Manufacturing teams.
- Evaluate LIMS data to provide ad hoc and long-term reporting solutions; identify process gaps and propose improvements.
- Write test scripts for new LIMS functionality and participate in validation of new functionality/releases.
- Develop and maintain process configurations based on end user procedures and requirements.
- Partner with the LIMS team, IT, and end users to ensure new functionality meets user requirements.
- Create and revise LIMS documentation: SOPs, Work Instructions, Design Specifications, and training materials.
- Support LIMS platform expansion by preparing and executing validation test scripts.
- Liaise with laboratory end users to ensure configuration changes meet user needs.
- Revise or develop Functional Requirement Specifications (FRS) and User Requirement Specifications (URS), plus other relevant documentation.
- Perform other related duties as assigned.
WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS
- Ability to sit for prolonged periods (approximately 240 minutes daily); perform repetitive motions with wrists/hands/fingers.
- Ability to lift/move objects up to 10 lbs.
- Ability to discern audible cues and perform tasks requiring 20/20 corrected vision, including color differentiation.
- No routine requirement for respiratory protection, working at heights, operating motor vehicles/PITs, or working in extreme temperatures.
BENEFITS
We offer a competitive, comprehensive benefits package designed to support your well-being and growth. Highlights typically include:
- Competitive compensation with performance recognition
- Medical, dental, and vision coverage
- Retirement savings plan with company contribution
- Paid time off, company holidays, and paid parental leave
- Education assistance, professional development, and training
- Employee assistance program and wellness resources
- Inclusive culture with employee resource groups and opportunities to contribute to continuous improvement
EQUAL OPPORTUNITY
We are an equal opportunity employer. We welcome applicants of all backgrounds and are committed to a fair, accessible, and inclusive hiring process. If you require a reasonable accommodation at any stage, please let us know.
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).
POSITION OVERVIEW:
Help build and optimize a best-in-class LabWare LIMS v8 environment that powers Quality Control in a GMP setting. As Sr. Specialist 1, QC LIMS, you’ll configure, validate, and sustain a critical system that enables compliant, efficient testing—directly impacting product quality and patient safety.
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.”
About us
We are a collaborative Quality Control LIMS team partnering closely with Quality Control, Analytical Development, Manufacturing, IT, and Quality Assurance. Our mission is to ensure our LabWare LIMS operates in a robust, validated, and compliant state aligned with cGMP, ICH, FDA, 21 CFR Part 11, and GAMP expectations. We value curiosity, accountability, and cross-functional partnership, and we foster an inclusive environment where every voice is heard and respected.
MINIMUM QUALIFICATIONS
- Bachelor’s degree in Computer Science, Information Technology, Biology, Microbiology, Biochemistry, or a related scientific discipline with 2+ years of experience; or
- Master’s degree in the same fields with 0 years of experience
- Ability to function in a fast-paced, highly technical environment
- Demonstrated ability to work cross-functionally and build strong partnerships across levels (management, laboratory personnel, plant personnel)
- Thorough knowledge of cGMP/ICH/FDA regulations; familiarity with 21 CFR Part 11 and GAMP
- Strong verbal and written communication, technical writing, and problem-solving skills
- Understanding of pharmaceutical/biotech testing cycles or requirements
- Ability to work effectively with diverse teams
PREFERRED QUALIFICATIONS
- 1–3 years of experience in a cGMP Quality Control department or FDA-regulated industry (drugs/biologics)
- Previous experience with LabWare LIMS development or other LIMS software development
- Experience with 21 CFR Part 11 and GAMP (applied/working experience)
- TrackWise (or similar quality system) experience for at least 1 year
- Leadership aptitude
Responsibilities
- Participate in the LabWare LIMS v8 site go-live, including static data migration, configuration, validation, and cross-functional coordination to ensure a successful rollout.
- Collaborate with business subject matter experts to define and document new or revised LabWare requirements.
- Configure basic and advanced LabWare LIMS objects, including:
- Specifications, Analyses, Batch Templates, Test Lists, QC Samples
- Calculations, Format Calculations
- Templates (Stability, Sample Login, Standards, Reagents)
- Execute qualification/verification testing to support implementation of new or revised LabWare configurations.
- Maintain and, when needed, repair configuration objects within LabWare LIMS.
- Create queries to support evolving business requirements.
- Use the change management system to update configurations for specifications, analyses, and other static data in LIMS.
- Provide timely user support and troubleshooting; create new configuration templates; maintain accurate change records per version control procedures.
- Deliver LIMS training, technical support, problem reporting, and resolution for QC, QA, AD, and Manufacturing teams.
- Evaluate LIMS data to provide ad hoc and long-term reporting solutions; identify process gaps and propose improvements.
- Write test scripts for new LIMS functionality and participate in validation of new functionality/releases.
- Develop and maintain process configurations based on end user procedures and requirements.
- Partner with the LIMS team, IT, and end users to ensure new functionality meets user requirements.
- Create and revise LIMS documentation: SOPs, Work Instructions, Design Specifications, and training materials.
- Support LIMS platform expansion by preparing and executing validation test scripts.
- Liaise with laboratory end users to ensure configuration changes meet user needs.
- Revise or develop Functional Requirement Specifications (FRS) and User Requirement Specifications (URS), plus other relevant documentation.
- Perform other related duties as assigned.
WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS
- Ability to sit for prolonged periods (approximately 240 minutes daily); perform repetitive motions with wrists/hands/fingers.
- Ability to lift/move objects up to 10 lbs.
- Ability to discern audible cues and perform tasks requiring 20/20 corrected vision, including color differentiation.
- No routine requirement for respiratory protection, working at heights, operating motor vehicles/PITs, or working in extreme temperatures.
BENEFITS
We offer a competitive, comprehensive benefits package designed to support your well-being and growth. Highlights typically include:
- Competitive compensation with performance recognition
- Medical, dental, and vision coverage
- Retirement savings plan with company contribution
- Paid time off, company holidays, and paid parental leave
- Education assistance, professional development, and training
- Employee assistance program and wellness resources
- Inclusive culture with employee resource groups and opportunities to contribute to continuous improvement
EQUAL OPPORTUNITY
We are an equal opportunity employer. We welcome applicants of all backgrounds and are committed to a fair, accessible, and inclusive hiring process. If you require a reasonable accommodation at any stage, please let us know.
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).
STEM OPT Distribution & Wholesale Job Roles in North Carolina
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Search Distribution & Wholesale Jobs in North CarolinaDistribution & Wholesale STEM OPT Sponsorship Jobs in North Carolina: Frequently Asked Questions
Which distribution and wholesale companies sponsor F-1 STEM OPT visas in North Carolina?
Large distribution and wholesale employers with significant North Carolina operations, including companies in Charlotte's logistics corridor and the Triad region's industrial base, have filed Labor Condition Applications for STEM-related roles. Companies in food distribution, industrial wholesale, and e-commerce fulfillment with data and systems functions tend to sponsor F-1 STEM OPT students. Checking OFLC employer filing history helps identify which specific companies have recent sponsorship records in the state.
Which cities in North Carolina have the most distribution and wholesale F-1 STEM OPT sponsorship jobs?
Charlotte leads in distribution and wholesale STEM OPT activity due to its role as a major Southeast logistics hub, with strong employer presence around its intermodal freight infrastructure. The Research Triangle, including Raleigh and Durham, offers roles tied to supply chain technology and analytics. Greensboro and Winston-Salem in the Triad region also have established wholesale and distribution employers, particularly in furniture, textiles, and food distribution.
What types of distribution and wholesale roles typically qualify for F-1 STEM OPT sponsorship?
Roles that qualify for F-1 STEM OPT sponsorship must fall under a STEM-designated Classification of Instructional Programs code matching the student's degree. In distribution and wholesale, qualifying positions typically include supply chain analyst, logistics data analyst, demand planning analyst, operations research specialist, and inventory optimization roles. Positions requiring quantitative methods, data systems, or engineering skills tied to a STEM degree are the most common qualifying categories. O*NET can help confirm whether a specific job title aligns with a STEM-eligible occupation.
How do I find distribution and wholesale F-1 STEM OPT sponsorship jobs in North Carolina?
Migrate Mate lets you search specifically for distribution and wholesale employers in North Carolina that have filed for F-1 STEM OPT workers, using verified OFLC data to show which companies have an active sponsorship history. This is more reliable than general job searches because it filters for employers who have already navigated the process. Narrowing results by city, role type, and STEM designation helps target companies in Charlotte, the Research Triangle, and the Triad area where this sector is most active.
Are there any state-specific or industry-specific considerations for F-1 STEM OPT sponsorship in North Carolina's distribution sector?
North Carolina distribution employers participating in federal contracting or with E-Verify enrollment are already set up to handle F-1 STEM OPT work authorization, since E-Verify participation is required for STEM OPT extensions per USCIS rules. The state's concentration of third-party logistics providers and wholesale distributors in the Charlotte and Triad regions means employer familiarity with OPT paperwork varies widely. Students should confirm that a prospective employer is E-Verify enrolled before accepting an offer, as this is a non-negotiable STEM OPT extension requirement.