Location: Minnetonka, MN
Duration: 9 months
- Working with CAPA project teams
- Assist with root cause investigations
- Assist in the development of Corrective Solutions
- Conduct and document verification testing Quality Systems Duties and
Qualifications:
- BS in Mechanical or Biomedical Engineering (preferred)
- Experience with CAPA
- Experience with medical device Design Controls including design verification and requirement documentation
- Strong technical writing skills
- 5 years minimum experience in Engineering position
- 2-3 years minimum experience in Medical Device Industry
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