Quality & Regulatory Specialist II
Trimedx(1 month ago)
About this role
The Quality & Regulatory Compliance Specialist II at TRIMEDX serves as a subject matter expert for medical device quality management and regulatory adherence across Field Operations. The role supports maintenance of the Quality Management System and regulatory programs to ensure compliance with applicable standards and accreditations. This hybrid position is based in the Indianapolis, IN region and requires regional residency and travel.
Required Skills
- ISO 13485
- Internal Audit
- Regulatory Compliance
- QMS
- CAPA
- Recall Management
- Risk Management
- Clinical Engineering
- Excel
- Microsoft Office
+2 more
Qualifications
- Bachelor’s Degree
- Associate Degree Consideration
About Trimedx
trimedx.comTRIMEDX delivers clinical engineering management through the clinical engineering services, clinical asset informatics, & medical device cybersecurity.
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