- Consult with Manufacturing, Information Management, Research Development & Engineering, Quality Assurance Operations, and Product Performance Analysis teams to ensure compliance with LifeScan software development procedures and industry regulations
- Review and approve deliverables of the software development lifecycle
- Lead teams in performing Hazard Analysis
- Occasionally assist teams in developing Standard Operating Procedures and Work Instructions for software development activities tailored to their specific needs
- Occasionally provide training for select software development activities for LifeScan
- Occasionally write and execute test protocols and reports
- Bachelor's degree in Engineering required, Mechanical Engineering or Biomedical degree is a plus
- Minimum of 3-5 years of experience required
- Attention to detail and proficiency in managing reports and regulatory compliance
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Quality Engineer - Temecula, United States - GForce Life Sciences
Description
Responsibilities:
Requirements: