Home › Companies › Uscareers Fujifilm Icims Com › Sr. QA Technical Specialist
Sr. QA Technical Specialist
Uscareers Fujifilm Icims Com · Research Triangle Park, NC, US · On Site · Deleted · iCIMS
Job facts
| Field | Value |
|---|---|
| Company | Uscareers Fujifilm Icims Com |
| Title | Sr. QA Technical Specialist |
| Normalized title | - |
| Department / team | Quality Assurance |
| Location | Research Triangle Park, NC, United States |
| Work model | On Site |
| Employment type | OTHER |
| Salary | - |
| Status | deleted |
| ATS provider | iCIMS |
| Posted / first seen | 2026-04-10 / 2026-05-31 |
| Changed / last seen | 2026-06-06 / 2026-06-03 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Uscareers Fujifilm Icims Com. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through iCIMS. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Research Triangle Park. | Open |
| Department jobs | Active postings in Quality Assurance. | Open |
| Work model jobs | Active On Site postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Uscareers Fujifilm Icims Com |
| Source | f8d75ae9-789d-4bc9-b0c7-b07ee3fba3e4 |
| ATS provider | iCIMS |
Description
Position Overview
The Senior QA Technical Specialist acts independently and provides QA subject matter knowledge in the GMP domain to systems and projects with focus on key quality activities and deliverables in accordance with company policies/SOPs and regulatory requirements. Works closely with project teams and stakeholders across the organization, support development and maintenance of computerized system and data integrity PQS subsystems.
Company Overview
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
Job Description
Major Accountabilities:
Review and approval of validation documentation against PQS subsystems Computerized Systems and Data Integrity processes and requirements.
Review and approval of qualification documentation against PQS subsystems Computerized Systems and Data Integrity processes and requirements.
Review and approval of changes, events/deviations, incidents, CAPAs etc. (process records) as well as procedural documents in relation to computerized systems.
General inspection and audit support in relation to computerized systems.
Develop and maintain the PQS framework related to computerized systems and based on current GMP and other relevant regulatory requirements (per global policies).
Meet internal training requirements (per assigned training curricula) and keep oneself up to date on current GMP and other relevant regulatory requirements as well as relevant guidelines for computerized systems
This position has interactions to Engineering as well as all other QA functions locally and globally.
Education and Experience Requirements:
High School Diploma or Equivalent with 12 years of applicable industry experience OR
Bachelor’s degree with 8 years of applicable industry experience OR
Master’s degree 6 years of applicable industry experience OR
PhD with 4 years of applicable industry experience
Solid GMP knowledge
Preferred Experience:
QA and/or manufacturing expeirence from the pharmaceutical industry
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.
*#LI-Onsite
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]).
Full job record
| Job ID | ec66f8b22485fdea8eeca5e45948331c708ce71d |
| Org ID | 51ab77ff-1617-41fc-aaef-c21d6b75e795 |
| Source ID | f8d75ae9-789d-4bc9-b0c7-b07ee3fba3e4 |
| Board ID | f8d75ae9-789d-4bc9-b0c7-b07ee3fba3e4 |
| Provider | icims |
| Provider Job Key | 37515 |
| Title | Sr. QA Technical Specialist |
| Normalized Title | — |
| Status | deleted |
| Active | no |
| Location Text | Research Triangle Park, NC, US |
| Department | Quality Assurance |
| Team | — |
| Employment Type | OTHER |
| Workplace Type | on_site |
| Remote Policy | — |
| Country | United States |
| Region | NC |
| City | Research Triangle Park |
| Salary Raw | Position Overview The Senior QA Technical Specialist acts independently and provides QA subject matter knowledge in the GMP domain to systems and projects with focus on key quality activities and deliverables in accordance with company policies/SOPs and regulatory requirements. Works closely with project teams and stakeholders across the organization, support development and maintenance of computerized system and data integrity PQS subsystems. Company Overview 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 Job Description Major Accountabilities: Review and approval of validation documentation against PQS subsystems Computerized Systems and Data Integrity processes and requirements. Review and approval of qualification documentation against PQS subsystems Computerized Systems and Data Integrity processes and requirements. Review and approval of changes, events/deviations, incidents, CAPAs etc. (process records) as well as procedural documents in relation to computerized systems. General inspection and audit support in relation to computerized systems. Develop and maintain the PQS framework related to computerized systems and based on current GMP and other relevant regulatory requirements (per global policies). Meet internal training requirements (per assigned training curricula) and keep oneself up to date on current GMP and other relevant regulatory requirements as well as relevant guidelines for computerized systems This position has interactions to Engineering as well as all other QA functions locally and globally. Education and Experience Requirements: High School Diploma or Equivalent with 12 years of applicable industry experience OR Bachelor’s degree with 8 years of applicable industry experience OR Master’s degree 6 years of applicable industry experience OR PhD with 4 years of applicable industry experience Solid GMP knowledge Preferred Experience: QA and/or manufacturing expeirence from the pharmaceutical industry 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. *#LI-Onsite 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]). |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | hour |
| Source URL | https://uscareers-fujifilm.icims.com/jobs/37515/sr.-qa-technical-specialist/job |
| Apply URL | https://uscareers-fujifilm.icims.com/jobs/37515/sr.-qa-technical-specialist/job |
| First Seen At | 2026-05-31 18:50:10Z |
| Last Seen At | 2026-06-03 14:36:07Z |
| Last Checked At | 2026-06-06 08:41:57Z |
| Last Changed At | 2026-06-06 08:41:57Z |
| Inactive At | 2026-06-06 08:41:57Z |
| Source Posted At | 2026-04-10 04:00:00Z |
| Source Updated At | 2026-04-10 18:57:52Z |
| Raw Payload Uri | s3://bluework-jobs-prod-raw-590183727216/raw/provider=icims/board=uscareers-fujifilm.icims.com/date=2026-06-03/2026-06-03T14-35-50-167Z-75519bb13a504ea6f0d1ac80482038943677a4ca97bae6ee23d97f4a64f44e3d.json |
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