Lumicity
Job Location :
Irvine,CA, USA
Posted on :
2025-08-04T03:07:10Z
Job Description :
Client: Medical Device
Project Details
- 12-Month contract. (Conversion likely).
- On-site, 5 days per week.
Responsibilities
- Provide expert QA guidance across design controls, specifications, test methods, usability, and risk management throughout product development.
- Lead product quality input in design reviews and maintain compliance documentation (DHF/DMR) per regulatory and SOP requirements.
- Drive risk management and human factors activities to ensure safe, user-friendly orthopedic device designs.
- Apply statistical and quality engineering tools for verification/validation planning, CAPA investigations, and continuous improvement initiatives.
- Support audits, regulatory submissions, and quality system processes related to design, risk, complaints, and CAPA.
Qualifications
- Bachelor's degree with 7+ years (or 15+ years without a degree).
- The ideal candidate should have hands-on experience in risk identification, design verification, and testing.
- ASQ Certified Quality Engineer. (Preferred).
Apply Now!