Top Tech Jobs & Startup Jobs

The Distinguished Engineer will lead and execute material characterization and testing for heart valve programs, focusing on metals and mechanical testing. Responsibilities include improving test setups, mentoring engineers, ensuring compliance with regulations, and collaborating with project teams to select materials for medical devices.

The Senior Analyst, Sales Strategy & Compensation will lead the development and implementation of U.S. sales incentive plans, manage the sales planning process, prepare commission statements, provide management decision support, develop presentations for management, and collaborate cross-functionally on ad hoc projects.

The Strategy Manager will lead annual strategic planning, develop impactful presentations for stakeholders, support strategic discussions at leadership meetings, evaluate local markets, and collaborate across functions to drive actionable strategic plans. This role also requires guiding project teams to address strategic challenges and fostering internal relationships.

The Supplier Quality Engineer II focuses on optimizing product development through supplier collaboration and quality assurance. Responsibilities include facilitating gage studies, developing test methods, conducting supplier audits, analyzing quality metrics, and managing non-conformances while ensuring compliance with industry standards.

The Senior Analyst will support the TMTT Sales Operations team by managing and enhancing case scheduling processes. This role involves collaboration with sales teams and stakeholders to optimize resource allocation, responding to scheduling inquiries, and developing KPI reports and dashboards. The position requires at least 5 years of experience in sales operations or project management within the medical device industry.

The Principal Statistical Programming role involves leading statistical programming for clinical trials using SAS and R, developing and validating programs, mentoring junior programmers, and ensuring compliance with regulatory standards.

As a Principal in Statistical Programming, you will develop, validate, and execute SAS programs for clinical trials, ensuring compliance with regulatory standards. You'll mentor junior programmers, collaborate with statisticians, and contribute to clinical report creation while maintaining documentation and quality control.