This is an immediate requirement. Please apply if you can join within 20 days or close to 20 days
Roles and Responsibilities:
Lead the project execution in compliance with design control SOP.
Work with cross functional teams to define device design and technology optimized for power modules.
Oversee all technical aspects of the development process including pertinent deliverables, statistically sound design verification protocols/reports, design validation activities, and support with human factors studies.
Support the optimization of design control elements to comply with medical device regulations.
Identification of user needs, product requirements and specification development, feasibility test development, design verification and validation testing, risk assessments, device creation, general project team technical support, and extensive collaboration with both internal stakeholders and external development partners.
Ensure product cost, performance, quality, yield and reliability goals are met.
Champion and apply Systems engineering principles in development and support continuous process improvement.
Generate and present technical information to multidisciplinary audiences (internal/external) and levels.
Collaborate with cross-disciplinary teams and external groups to coordinate and drive complex studies
Travel to study sites and testing labs to support study execution and monitor progress.
