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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, applicable

ISO 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. Identify all Customer Complaints, take appropriate action and maintain all records. Escalate all potential reportable events to Product Safety Committee, Regulatory Affairs and Quality Assurance. Process all Customer Complaints in the quality management system. Interact closely with Customer Service, Service, Repair, Research and Development, Quality Assurance, Regulatory Affairs and Sales to facilitate required action. Perform Corrective and Preventive Action activities as needed. Support other Quality Management System activities as they relate to Customer Complaints (CAPAs, Non-conformances, internal/external audits, remediation activities) Support other Regulatory Affairs activities as they relate to Customer Complaints (adverse event reporting, field actions). Attend all department and company-wide team meetings as needed. Other duties as assigned. Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable

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 support activities in a

U.S. FDA

regulated environment. Deep knowledge of

U.S. FDA

medical device regulations (21 CFR 820, 21 CFR 803, 21 CFR 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. The ability to use your hands and fingers to feel and manipulate items, including keyboards, up to 100% of applicable work time. The ability to stand, talk, and hear for 75% of applicable work time. The ability to lift and carry up to ten pounds up to 20% 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 •#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 the

COVID-19

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Find & Apply For Regulatory Affairs Specialist Jobs in Twinsburg, Ohio

Complaint Handling Specialist (Twinsburg, OH)