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Manufacturing Specialist 1 Production Schedule

Job Location:

Holly Springs, MS - USA

Monthly Salary: Not provided by the employer

Posted: 19 July 2026 (30+ days ago)

Application Deadline: 16 October 2026

Vacancies: 1 Vacancy

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Job Summary

Position Overview

Help power life-changing biologics by orchestrating the heartbeat of our Drug Substance Manufacturing (DSM) operations. As the Production Scheduler youll own the daily and long-term production schedule drive schedule adherence and coordinate activities across Maintenance MSAT (Manufacturing Science and Technology) Engineering Quality Supply Chain and morekeeping people materials and equipment moving in sync.

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 mission-driven biologics organization committed to operational excellence and patient DSM we convert science into reliable cGMP-compliant production. This role is a central connectorpartnering closely with leaders and coordinators across departments to ensure timely production efficient resource use and a proactive response to change.

Work at the intersection of people and process to ensure schedule integrity and on-time performance
Collaborate across Manufacturing Planning Maintenance Quality Supply Chain Facilities Dispensary MSAT and Engineering
Use data and dashboards to inform decisions and drive continuous improvement in a fast-paced regulated environment
Foster a culture of safety quality and inclusion where every voice contributes to success

Responsibilities

Develop and manage finite detailed production schedules based on demand forecasts inventory goals and equipment and labor capacity
Run a daily production schedule cadence to drive schedule adherence and coordinate non-process activities with Maintenance MSAT Engineering Facilities and other partners
Monitor execution of production schedules; proactively adjust in response to delays equipment issues deviations or changing priorities
Communicate schedule updates risks and mitigation plans clearly and promptly to stakeholders and leadership
Coordinate with materials management to plan material usage (including solution lot records) and align material availability with production needs
Partner with cross-functional teams (Manufacturing Planning Quality Supply Chain Facilities Dispensary) to align activities and meet operational objectives
Contribute to long-term capacity planning and resource forecasting in support of strategic business initiatives
Design develop and maintain data dashboards and reports that enable effective decision-making; leverage tools such as Tableau and/or Alteryx (or similar)
Provide user training on the production system; develop and maintain associated business processes work instructions and user guides
Participate in daily and weekly planning meetings to support real-time operational decisions and issue resolution
Drive problem-solving for production schedule challenges facilitating collaborative solutions with leaders and coordinators across departments

Minimum Qualifications

High school diploma with 9 years of related experience; or
Associates degree in Life Science Engineering or a related field with 7 years of direct experience; or
Bachelors degree in Life Science Engineering or a related field with 5 years of direct experience
Equivalent military experience or training will be considered

Preferred Qualifications

Previous experience in biologics manufacturing
Proficiency in Tableau and/or Alteryx (or similar analytics/ETL and visualization software)
5 years of direct experience in current Good Manufacturing Practices (cGMP)

Knowledge Skills and Abilities

Strong knowledge of production planning and scheduling principles within a GMP-regulated manufacturing environment
Ability to analyze production data understand end-to-end process flows and deliver effective front-end reporting/dashboard solutions
Strong analytical problem-solving and organizational skills with high attention to detail
Effective communication and interpersonal skills with the ability to work confidently with leaders and cross-functional teams
Proven ability to manage multiple priorities in a fast-paced environment
Working knowledge of pharmaceutical or biotech operations (preferred)
Demonstrated ability to influence and drive resolution of production schedule challenges with diverse stakeholders

Inclusive culture that values safety quality collaboration and continuous learning
Competitive compensation with performance recognition
Comprehensive health and wellness programs
Retirement savings plan with employer support
Paid time off leave programs and flexible scheduling where role-appropriate
Professional development support including training and certification opportunities
Tools and technology to succeed (analytics platforms dashboarding and planning systems)
Opportunities to impact capacity planning and strategic operations

We are an equal opportunity employer. We welcome candidates of all backgrounds and experiences and provide reasonable accommodations throughout the hiring process. If youre passionate about coordinating complex operations love solving problems with data and thrive on cross-functional collaboration wed love to hear from you.

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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