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The Sr. Engineer, Supplier Development leads manufacturing engineering support for implantable devices, ensuring DFM, supplier qualification, and product integration in collaboration with cross-functional teams.

Lead the biostatistics team and manage clinical trial design and analysis while ensuring compliance, process improvement, and stakeholder communication to achieve optimal patient outcomes.

The Senior Supplier Quality Engineer leads qualification efforts for supplier components, collaborates with cross-functional teams, and develops testing methods, ensuring product quality and regulatory compliance.

The Engineer I will provide technical support for implantable heart monitoring technology, focusing on troubleshooting, data analysis, and collaboration with R&D and other teams.

Manage product master data for accuracy and consistency, collaborate with stakeholders, establish data governance, and lead councils for data quality improvements.

The Senior Director will lead and oversee the US compliance program, ensuring adherence to healthcare compliance and regulations while collaborating with various stakeholders.

Lead financial planning and analysis, provide executive guidance, support growth initiatives, mentor junior staff, and drive process improvements.