CQV Engineer 2

Fujifilm

Job Location:

Holly Springs, MS - USA

Monthly Salary: Not Disclosed

Posted on: 9 hours ago

Vacancies: 1 Vacancy

Job Summary

Position Overview

The CQV Engineer 2 supports the commissioning and qualification of equipment and systems for the site. This role coordinates with the CQV team to perform validation activities to include but not limited to equipment set up building dashboards and reading and reviewing documents. This role ensures equipment and systems comply with regulatory requirements and quality standards.

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

Configures tests and validates electronic systems to ensure the systems are properly qualified and validated per standards and regulatory requirements (e.g. Food & Drug Administration (FDA))
Reads piping & instrumentation diagrams (P&IDs) to walkthrough systems in the field
Drafts and implements validation protocols
Coordinates the execution of validation activities (e.g. equipment set up material readiness and work orders)
Creates work orders generates calibration reports maintenance plans and other items in the computerized maintenance management system (CMMS)
Executes validation protocols for manufacturing equipment lab and admin process support equipment etc.
Develops dashboards in Tableau to visualize and analyze CQV data to track progress and trends
Identifies potential risks and escalates to senior engineers or management for resolution
Creates implements and maintains equipment and system qualifications and validation protocols
Prepares and presents report packages for implementation into standard operating procedure (SOPs)
Prepares validation master plans for facilities equipment and systems
Other duties as assigned

Minimum Qualifications:

Bachelors degree in Engineering with 2 years of experience in validation activities in facilities commissioning and systems qualifications

Preferred Qualifications:

Masters degree in Engineering with no prior experience
Prior experience with Good Manufacturing Practices (cGMP) or working in another highly regulated industry
Prior experience with mammalian cell culture process

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:

Position OverviewThe CQV Engineer 2 supports the commissioning and qualification of equipment and systems for the site. This role coordinates with the CQV team to perform validation activities to include but not limited to equipment set up building dashboards and reading and reviewing documents. Thi...