Job Description
A medical device client of ours is seeking Entry Level Biomedical Engineers. This role will ensure compliances with GMPs as well as review complaints of a field experience with implanted devices.
Job Duties:
- Evaluate complaints regarding medical device products and determine if further investigation is necessary
- Perform complaint investigations, document investigation results, and maintain records of investigation using global complaint handling system and documented quality system in compliance with FDA 21 CFR Part 820 and ISO 13485:2003
- Assess complaints regarding products for MDR/ADR reportability using global complaint handling system and documented quality system in compliance with FDA 21 CFR Part 820 and ISO 13485:2003
Job Qualifications:
- BS Biomedical Engineering is preferred, however other Engineering disciplines are also acceptable
- Biomedical related internships are highly preferred
- Proficiency using Microsoft Excel
For consideration, please apply directly to this posting or email your resume to [Click Here to Email Your Resum]
Experis is an Equal Opportunity Employer (EOE/AA)
Job Requirements
Country: USA, State: Minnesota, City: Minneapolis, Company: Experis.
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