Position Overview
The Sr CQV Engineer 1 leads the commissioning and qualification of equipment and systems of assigned area for the site. This role performs and leads the CQV team through the validation lifecycle, investigation of deviations and root cause analyses, and establishes standard operating procedures and other documents. This role collaborates with internal and external stakeholders to ensure strategies, equipment, and systems incorporate global standards and
align and comply with regulatory requirements and quality standards. Additionally, this role provides training and guidance to junior engineers to ensure successful integration of CQV activities into site projects.
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: ;br>
Job Description
What You'll Do
Acts as CQV Technical Lead for process support equipment to establish validation strategies, develop validation procedures that align with FDB's
Large Scale Biologics platform operating principles and regulatory requirements
Provides guidance and leads the management of validation lifecycle for responsible areas for process support equipment and warehouse during
Installation Verification (IV), Operational Verification (OV), Installation & Operational Qualification (IOQ), Performance Qualification (PQ) through
Good Manufacturing Practices (GMP) release to decommissioning
Provides technical support and leads external validation engineers through commissioning, qualification and validation of Large-Scale Biologics
facilities and equipment
Participates with FDB's cross-network to inform and influence strategic management of validation programs, and working knowledge to
incorporate global standards at the site level
Liaises and collaborates with key stakeholders and support groups (e.g., Manufacturing, Process Science, Automation, Supply Chain, and Quality) to
ensure FDB validation requirements are met
Collaborates cross-functionally to ensure successful integration of CQV activities into projects
Establishes Validation standard operating procedures (SOPs), Validation Project Plan (VPP), and Validation Master Plan (VMP) to ensure full cGMP
compliance by operations launch
Liaises with CQV Document Generation Lead to generate and approve DQ, Design Reviews, SLIA, Test Matrices, Risk Assessments, QA Vendor
Assessments, FAT, SAT, CTP, and IOQ Protocols
Leads the investigation of qualification deviations or discrepancies utilizing problem solving, and root cause analysis (RCA) to properly identify root
causes and develop remediation plans (e.g., corrective and preventive action (CAPAs))
Performs change control validation assessments to determine risk-based qualification, requirements for new systems, and changes to existing
qualified systems
Conducts impact and risk assessments and identifies risks and develops and leads the implementation of mitigation strategies
Provides guidance and training to junior engineers for all CQV-related activities, as needed
Other duties, as assigned
Minimum Requirements:
Bachelor's degree in Engineering
8 years of experience in validation activities in facilities,
commissioning, and systems qualifications
Experience with cGMP or working in another highly regulated
industry
Preferred Requirements:
Master's degree in Engineering with 6 years of experience in
validation activities in facilities, commissioning, and system
qualifications
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 ().
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
- Dice Id: 80183352
- Position Id: 3df621db3b8e96d48bff1a06c5682e4d
- Posted 21 hours ago
