QA Specialist, PQS

Holly Springs, MS - USA

Monthly Salary: Not Disclosed

Posted on: 8 hours ago

Vacancies: 1 Vacancy

Job Summary

Position Overview

The QA Specialist PQS is responsible for the day-to-day activities of the Pharmaceutical Quality Systems team. This role requires system expertise and business knowledge to act as point of contact and maintain deep understanding of the system and process functionality/improvements and how they apply locally and globally to the system(s). The role collaborates and establishes relationships with site-based customers and global colleagues and provides updates to leadership as requested. As a system SME the QA Specialist PQS assists with user management user support problem solving and system training.

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

What Youll Do

Supports QA for project deliverables in accordance with the governing processes and procedures within the assigned Quality area
Assesses the impact of system controls and process modifications and maintains oversight of change management processes
Provides Quality/GMP oversight and approval of assigned area/systems and processes lifecycle documentation including risk and impact assessments product process and equipment specifications functional specifications traceability matrices qualification protocols validation plans and validation summary reports
Reviews and approves QA procedures for the validation approach and lifecycle documents as assigned
Generates reviews and approves QA documentation procedures and processes for operational readiness objectives and QA support of assigned area/systems in cGMP regulated facility
Ensures project and operational quality objectives are met within desired timelines
Actively seeks opportunities to collaborate and align with other FUJIFILM Diosynth Biotechnologies sites to streamline processes and maximize efficiency
Supports quality decisions that may impact operations ensuring appropriate escalation
Identifies risks and communicates gaps for quality and GMP process/systems
Performs other duties as assigned

Minimum Requirements:

BS/BA in Life Sciences or Engineering or equivalent with 2 years of applicable industry experience OR
Masters in Life Sciences or Engineering with 0 years of applicable industry experience.
1-3 years of experience in a GMP environment

Preferred Requirements:

Prior experience working within a QA role preferred

Working Conditions & Physical Requirements:

Will work in environment which may necessitate respiratory protection X No Yes
May work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program. X No Yes
Will work in environment operating a motor vehicle or Powered Industrial Truck. X No Yes
Ability to discern audible cues. No x Yes
Ability to inspect or perform a task with 20/20 corrected vision visual acuity including distinguishing color. X No Yes

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 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 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 QA Specialist PQS is responsible for the day-to-day activities of the Pharmaceutical Quality Systems team. This role requires system expertise and business knowledge to act as point of contact and maintain deep understanding of the system and process functionality/improvements a...