Auditor/Product Expert for Non Active Medical Devices (m/f/x)
TÜV Rheinland Group
- Experience
- 2+ yrs
- Location
- United States
- Job type
- Full-time
About the role
Degree in natural sciences, medical or engineering; 2+ years professional experience in medical device development, production, QA, regulatory affairs or quality management; knowledge of EN ISO 13485, ISO 9001, MDSAP, TCP; fluent English; Class B driver's license; up to 70% travel.
About TÜV Rheinland Group
Global provider of technical inspection, testing, and certification services.
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