Role: Quality Engineer I (Medical Device)
Location: Westbrook, ME
Duration: 5 Months on
W2
Shift Timings: 6 AM to 2:30 PM
#On-Site
Job Description
- Consult with Manufacturing, Information Management, R&D, Quality Assurance, and Product Performance teams for compliance with LifeScan software development procedures and regulations.
- Review and approve software development lifecycle deliverables.
- Lead Hazard Analysis and occasionally assist in developing SOPs and Work Instructions for software development.
Provide training for software development activities and write/execution test protocols and reports as needed.