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The Talent Acquisition Partner is responsible for sourcing exempt and non-exempt positions, managing recruiting strategies, and collaborating with HR partners to ensure effective staffing.

Lead quality assurance initiatives, develop and maintain quality standards, analyze design changes, and manage validation processes for medical devices. Supervise teams and conduct audits for compliance.

The Senior Commercial Product Development Director leads the commercial aspects of product development, overseeing pricing strategies, business case approvals, and managing a portfolio of medical device development programs.

The Senior Manager, Commercial Finance will analyze pricing strategies, forecast revenue, maintain financial data, and lead a team to optimize profitability and support commercial decisions.

As a Quality Assurance Engineer I, you will develop and maintain quality standards, design inspection methods, analyze product issues, and ensure compliance with regulations, while providing technical guidance and participating in audits.

Develop and optimize surface processes for Nitinol medical devices, collaborating with teams and creating manufacturing documentation while applying six sigma and lean principles.

The Senior Staff Process Development Engineer will lead process improvements, validation, and new product introductions for medical devices, focusing on extrusion and balloon development.

The Manufacturing Engineer I develops and sustains production methods, ensures compliance with safety standards, conducts inspections, and optimizes manufacturing processes.

The Manufacturing Engineer is responsible for process improvements, compliance with regulations, and overseeing production efficiency while mentoring lower-level personnel.

The Manufacturing Engineer II ensures compliance with safety regulations, develops manufacturing methods, conducts quality inspections, and implements efficiency improvements in medical device production.