About the role
Quality Engineer II
Location: Menlo Park, CA (Onsite)
Shift: 2nd Shift (Approx. 3:00 PM – 1:00 AM)
Role Summary
Seeking a Quality Engineer II to support manufacturing quality activities in a medical device environment. The role involves investigating quality issues, supporting nonconforming material reviews, driving root cause analysis and CAPA, monitoring manufacturing processes, and ensuring compliance with quality system and regulatory requirements.
Key Responsibilities
- Support manufacturing quality and process improvement initiatives.
- Investigate nonconforming material, scrap, and quality issues.
- Perform root cause analysis and support CAPA activities.
- Monitor manufacturing processes and quality metrics.
- Assist with product release, risk assessments, and quality documentation.
- Collaborate with Manufacturing, Operations, and R&D to resolve quality issues.
- Ensure compliance with FDA, GMP, and Quality System requirements.
Qualifications
- Bachelor's degree in Engineering or a related technical field.
- 2–5 years of Quality Engineering experience in a regulated manufacturing environment.
- Experience with CAPA, root cause analysis, nonconforming material, and quality systems.
- Familiarity with FMEA, SPC, and continuous improvement tools.
- Medical device industry experience is preferred.
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