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Fujifilm
Complaint Handling Specialist
Career Insights for Regulatory Affairs Specialist
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What they do
A Regulatory Affairs Specialist maintains specialized knowledge of state and federal government regulations that affect an employer. Interprets regulations and implements procedures that bring an employer into compliance with regulations; may audit internal compliance with regulations.
$97,974 / year median in the U.S.
+1% projected growth
Job Description
- Position Overview
- This position is intended to provide Complaint Handling support to
FUJIFILM
Healthcare Americas Corporation. This position supports full, ongoing compliance to all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicableISO 13485
standard requirements and all other applicable laws, regulations, and standards.- Company Overview
- At
FUJIFILM
Healthcare Americas Corporation, we're on a mission to innovate for a healthier world, and we need passionate, driven people like you to help us get there. Our cutting-edge healthcare solutions span diagnostic imaging, enterprise imaging, endoscopic and surgical imaging, as well as in-vitro diagnostics. But we don't stop at healthcare; our Non-Destructive Testing (NDT) team harnesses advanced radiography solutions to keep transportation infrastructure, aerospace, and oil and gas assets safe and running smoothly. Ready to innovate, collaborate, and make a difference? Join us and bring your big ideas to life while working in a dynamic, flexible environment that fuels your creativity and drive. Our headquarters is in Lexington, Massachusetts, an inspiring healthcare research hub in a historic town. 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
- Duties and responsibilities
- + Evaluate all sources of incoming customer information, identify, investigate and document customer complaints, perform trend analysis and maintain all records.
ISO 13485
standard requirements and all other applicable laws, regulations and standards.- Qualifications
- Experience + Three (3) or more years of hands on experience performing Quality System supportactivities in a
U.S. FDA
regulated environment. + Deep knowledge ofU.S. FDA
medical device regulations (21 CFR 820, 21 CFR 803, 21CFR 806, 21 CFR 807). + Deep knowledge of international medical device standard requirements (ISO 13485/ISO 9001, ISO 14971, EU Medical Device Directive and Canada Medical Device Regulations). Educational Requirements + Bachelor Degree highly preferred.Special Skills or Other Job Requirements:
+ Excellent leadership, communication, collaboration, team work and interpersonal skills + Superb ability to effectively communicate with staff members and business partners at all levels of the organization (both internal and external). + Excellent computer and internet search skills. + Strong ability to multi-task and to meet business deadlines. + Excellent organizational skills with an ability to think proactively and prioritize work.- Physical requirements
- The position requires the ability to perform the following physical demands and/or have the listed capabilities: + The ability to sit up 75-100% of applicable work time.
Close Vision:
The ability to see clearly at twenty inches or less.- Travel
- + Occasional (up to 25%) travel may be required based on business need
Salary and Benefits:
- + $73,759.00 - $82,000.00 + 8% Bonus opportunity + Medical, Dental, Vision + Life Insurance + 401k + Paid Time Off _
- #LI-Remote_ _In the event that
COVID-19
vaccine mandates issued by the federal government, or by state or local government become effective and enforceable, the Company will require that the successful candidate hired for positions covered under relevant government vaccine mandate(s) be fully vaccinated against COVID-19, absent being granted an accommodation due to medical or sincerely held religious belief or other legally required exemption._ _Applicants to positions where vendor credentialing or other similar requirements exist to enter facilities will be required to comply with the credentialing requirements of the facilities, including complying with vaccine requirements._ _For all positions, the Company encourages vaccination against COVID-19 and requires that the successful candidate hired be willing to test for theCOVID-19
virus periodically and wear a face covering indoors as required, absent being granted an accommodation due to medical or sincerely held religious belief or other legally required exemption._- 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 (hcushr.department@fujifilm.com or (330) 425-1313). Software Powered by ICIMS
- Job Locations
- _US-Remote_
- Posted Date
- _2 weeks ago_ _(8/12/2026 12:41 PM)_
- _Requisition ID_
- _2026-38318_
- _Category_
- _Regulatory/Compliance_
- _Company (Portal Searching)_
- _