In this role, you have the opportunity to lead on setting Quality and Reliability targets for IGT Systems medical software so that these innovative products deliver high quality and outstanding reliability to the lives they will improve. You are responsible for ensuring that appropriate project plan and quality plans are made, validating key design inputs, and providing effective oversight during the execution of the Quality Plan.
Requirements
- Bachelor’s engineering degree with 12 years / Master’s degree with 10+ years of experience
- Software testing experience
- Ability to define detailed software quality and reliability plans for new medical product developments
- Ability to contribute to Risk Management and lead FMEA activities for new products
- Strong exposure to application of Design Controls
- Ability to partner with V&V teams to assure thorough Verification, Validation and Useability testing
- Well conversant with statistical data analysis, regression modeling, reliability growth assessment and other quality techniques
- Experience with adequate and accurate review of DHF and DMR documents
- Understanding of global medical device regulations, requirements, and standards
- Experience with working in multidisciplinary teams in a high-tech R&D environment
- Effective interpersonal, written and oral communication skills
- Ability and willingness to work onsite
Benefits
- Health and wellness programs
- Professional development opportunities
- Diversity and inclusion initiatives