Pay Range: $40 - 48/hr depending on experience
Contract: 8 months with possible extension and/or conversion
100% onsite in Scarborough, ME OR possible remote for a strong candidate
Job Description:
- Coordinate non conformance incidents in FDA regulated devices.
- Conduct impact assessments & root cause investigations.
- Develop and close corrective action plans.
- Communicate across QA, engineering, and other functions.
- Contribute to Material Review Board discussions.
Qualifications:
- Bachelor's degree or higher required
- At least 3+ years of relevant quality experience
- Medical device industry needed
If you are interested in hearing more about the position, please respond to this posting with your resume attached or contact me at 813-356-0199.
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