Location: Phoenix, AZ
Job Summary:
Job Duties and Scopes
- Evaluate and investigate product complaints.
- Produce and complete Safety/Compliance Engineering documents.
- Perform safety/compliance engineering tasks such as assessing designs and completing root cause analysis.
Required Skills
- Basic understanding of Corrective Action Preventative Action (CAPA).
- Familiarity with global medical device regulations and standards (21 CFR Parts 803, 806, 820, ISO13485, ISO9001).
Required Experiences
- 5+ years of experience in the medical device industry.
- Bachelor’s degree in biomedical engineering, healthcare, nursing, or a related technical field.
Job URLs: