Engineering Documentation Specialist

Fujifilm • Holly Springs, NC

3d • Onsite

About The Position

The Engineering Documentation Specialist demonstrates a complete and thorough understanding of Engineering turnover documentation and is responsible for day-to-day document management activities in a paperless environment. This role processes incoming and outgoing documents, including receipt, classification, registry, distribution, archive, storage, and retrieval. This role also serves as the administrator for the project documentation management system and the subject matter expert (SME) for the Good Manufacturing Practice (GMP) Engineering Management system. FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By the 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.”

Requirements

• High School Diploma or GED with 9 years of document management experience (5 in the biopharmaceutical industry)
• Associate’s degree in engineering or related field with 7 years of document management experience (5 in the biopharmaceutical industry)
• Bachelor’s degree in engineering or related field with 5 years of document management experience in the biopharmaceutical industry

Nice To Haves

• Bachelor’s degree in engineering or related field with 9 years of experience working in an engineering-based EDMS
• Experience with equipment tagging and standards
• Experience with complex projects and working in operating facilities

Responsibilities

• Organizes, compiles, and maintains engineering and facility documentation (e.g., equipment documentation, facility drawings, specifications, etc.)
• Maintains documentation for existing equipment and manages approval workflows ensuring data integrity and audit readiness
• Processes project related documentation and turnover packages to ensure completeness, traceability, and seamless transition to operations
• Maintains departmental standard operating procedures (SOPs), monitors adherence across project teams, and enforces approved document control procedures
• Manages transmittals and issues to external stakeholders – and defining submittal protocols and standards (e.g., naming conventions, etc.)
• Collaborates with external Document Controllers ensuring compliance to established policies and procedures
• Identifies opportunities to enhance document control processes and right-first-time quality
• Integrates project management and quality principles within the document control function
• Assists the Building Information Modeling (BIM) team with documentation, including model/drawing standards and execution plans
• Partners with IT to configure, update, and sustain Electronic Document Management System (EDMS)
• Delivers training and user enablement for all EDMS and provides technical guidance to stakeholders, as needed
• Performs other duties, as assigned

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED