Complete all aspects of regulatory compliance testing, design reviews on complex projects, technical documentation review as per European MDR, & reporting on medical device client products & others. Participate in setting technical direction; plan schedule & coordinate detailed phases of a project. Train other test engineers & test technicians. Prepare test development project quotes & proposals by assisting in defining customer technical requirements, test strategies & selecting test equipment. Establish & maintain professional relationship with customers. Consult with customer on highly complex issues. Liaise with other global laboratories to ensure consistency & accuracy of methods & interpretations. Document test results for correction actions, reports & audits. Analyze test data & determine expected outcome for tests. Identify & report all deviations. Maintain confidentiality of all client information.
Requirements:
Bachelor's degree in Electrical or Electronics Engineering (or foreign equivalent) & 5 years of experience evaluating medical products in accordance with regulatory standards requirements, including experience with UL, CSA, IEC, EN, ISO standards. Brief domestic travel required.
Application Instructions:
Email resumes to TUV Rheinland of North America, Inc., Attention: careers@us.tuv.com.
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