Specialist 2, Quality Assurance Technical

Fujifilm • Research Triangle Park, NC

1d • Hybrid

About The Position

The QA Technical Specialist II performs final disposition of GMP raw materials and consumables to ensure timely availability for manufacturing. Serving as the QA point of contact for Warehouse, Supply Chain, and QC Raw Materials, this role resolves material-related issues and escalations, conducts quality impact assessments for investigations, change controls, and supplier change notifications, and ensures compliance with applicable procedures and data integrity requirements.

At FUJIFILM Biotechnologies, we’re leading the charge in advancing tomorrow’s medicines. If you want to be a part of life-impacting projects alongside today’s most innovative biopharmaceutical companies, FUJIFILM Biotechnologies could be the right place for you. From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on collaboration, creativity, and purpose. Whether your expertise lies in research, manufacturing, or production, you’ll find a home here where your efforts directly improve patients’ lives. Together, let’s shape the future of healthcare. Situated at the cross-section of Morrisville and Research Triangle Park (RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top universities, vibrant communities, and various outdoor opportunities. 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

Requirements

• High School Diploma or equivalent with 9+ years applicable industry experience; OR Associate’s degree with 7+ years; OR Bachelor’s degree with 5+ years; OR Master’s degree with 3+ years.
• Hands-on experience with SAP (material status/transactions) and Microsoft Office.
• Experience working within GMP quality systems (deviations, change control, investigations).
• Strong written and verbal communication, organization, critical thinking, and attention to detail.
• Demonstrated ability to multitask, prioritize, and meet timelines in a GMP environment.

Nice To Haves

• Bachelor’s degree with 5+ years applicable industry experience.
• TrackWise experience for deviations and change management.
• Supplier quality and/or material control experience in a regulated manufacturing environment.
• Proven ability to influence and collaborate across Supply Chain, QC, and QA.

Responsibilities

• Execute QA disposition of GMP raw materials and consumables to support manufacturing schedules.
• Update and manage material status and associated records in SAP.
• Contribute to and review quality system records (e.g., deviations, change management, change controls) in TrackWise.
• Perform quality impact assessments for investigations and supplier change notifications related to raw materials/consumables.
• Collaborate with Warehouse, Supply Chain, QC Raw Materials, and Quality leadership to resolve issues, drive timely decisions, and maintain flow of materials.
• Review and adhere to applicable SOPs and work instructions; identify and support procedural improvements.
• Uphold data integrity and ensure compliance with 21 CFR Part 820 and Part 11, and internal quality standards.

Benefits

• medical, dental, vision and prescription drug coverage with the option of a Health Savings Account with company contributions.
• industry leading 401(k) savings plan
• insurance coverage
• employee assistance programs
• various wellness incentives
• paid vacation time, sick time, and company holidays.

What This Job Offers

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