What are the responsibilities and job description for the Development Quality Engineer / Medical Device position at Intellectt Inc?
Role: Development Quality Engineer / Medical Device
Location: Pleasanton, CA
Duration: 12 Months (W2)
Key Responsibilities:
- Support development and quality assurance of medical device software
- Perform software verification and validation for updates and fixes
- Investigate and troubleshoot escalations and field issues
- Prepare for product releases and assist with post-release support
- Collaborate with cross-functional teams, including engineering, tech support, and field representatives
- Develop test plans, test cases, and execute software testing
- Attend meetings and communicate with various stakeholders
- Assist in product launch activities and post-launch monitoring
Required Skills & Qualifications:
- Experience in software verification, validation, and testing
- Strong troubleshooting and root cause analysis skills
- Ability to collaborate with software teams and cross-functional groups
- Solid technical foundation and eagerness to learns
- Medical device industry experience preferred due to regulatory requirements
Education & Experience:
- Bachelor’s degree in Computer Science, Biomedical Engineering (software-focused), or a related technical field preferred
- Minimum one year of industry experience preferred
- Strong internship experience may substitute for industry experience
Overqualification Considerations:
- Candidates with a Master’s degree may be considered overqualified
- The role is technician-focused rather than an engineering-level position
