Senior Specialist - Stability TS & SS

Position Overview

The QC Program Management Technical Support (TT) and Sample Support (SS) Senior Specialist 2 provides technical leadership through effective project management of the QC Sample Plans, QC Specifications, stability protocols, stability reports, stability sample pull scheduling, and stability specifications in close collaboration with relevant stakeholders and customers. This role helps ensure the timely completion of project milestones and deliverables, supports GMP compliant laboratory operations in accordance with regulatory guidelines, and participates in audits and inspections. As representative of QC, the TT/SS Senior Specialist 2 interfaces with customers to scope QC Sample Plans, QC Specifications and stability studies as well as participates in and leads collaborations with cross-functional teams.

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:

• Works in collaboration with customers and stakeholders from QC, Drug Substance Manufacturing (DSM), and Drug Product (DP) fill/finish to support tech transfers of new customer projects as they relate to QC Sample Plans, Stability studies, and DS/DP Specifications• Authors, reviews, and leads updates of controlled GMP documents related to QC Sample Plans, QC Specifications, Stability protocols, reports, and stability specifications• Leads, authors, and reviews change controls of QC Sample Plans and stability protocols for both internal and external changes together with relevant stakeholders, including communication with customers as applicable• Manages and directs the continuous improvement of QC Sample Plans and QC Specifications• Applies a holistic quality system approach through identifying and solving technical compliance gaps and areas for improvement or remediation related to quality or process; leads through completion and sustainable implementation• Leads/participates in team compliance activities including writing, changing, and maintaining GMP documents in collaboration with relevant stakeholders and QA• Ensures compliance with platform, procedures, and global QC vision• Supports management in training compliance with policies and inspections• Supports regulatory requests, audits, and inspections• Collaborates with the Laboratory Information Management System (LIMS) team and IT department to build DS/DP sample plan, specification, and stability functions that meet end-user and customer requirements• Provides guidance and feedback for QC personnel development• Performs other duties as assigned

Minimum Requirements:

• Bachelor’s degree in Microbiology, Virology, Biology, Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 5+ years of experience; OR• Masters degree in Virology, Microbiology, Biology, Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 3+ years of related experience; OR• Ph.D. in Virology, Microbiology, Biology, Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 0+ years of related experience• 5+ years of project management experience• 1-3 years of experience in a GMP environment• 2-3 years of Stability study management and protocol issuance• Experience with customers and tech transfers

Preferred Requirements:

• 5+ years of project management experience in biotechnology, Pharma, Contract Research Organization (CRO), or Contract Laboratory Organization (CLO)• Experience with Customer Relationship Management• Drug substance or manufacturing experience, including process validation, transfer, commercialization, and manufacturing support and troubleshooting• Experience using quality systems (e.g., deviation management system, change control, corrective and preventive action (CAPA), document management system)

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 ([email protected]).