Location: Phoenix, AZ
Job Summary:
Job Duties and Scopes:
- Evaluate and investigate product complaints.
- Produce and complete Safety/Compliance Engineering documentation.
- Perform safety/compliance engineering tasks, including assessing designs, reviewing tests, and conducting root cause analysis.
Required Skills:
- Basic understanding of Corrective Action Preventative Action (CAPA).
- Knowledge of global medical device regulations (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 related technical field.
Job URLs: