What You Will Do:

  Lead cross‑functional Stryker engineering teams to design, develop, and deliver innovative, life‑saving medical devices.

• Lead a cross-functional Engineering, Test, Quality, Manufacturing, Regulatory, Clinical, Compliance, Marketing and Project Management to ensure end to end project success including research, planning, development, testing, regulatory submittal, configuration management, manufacturing and service support.
• Proactive project planning includes identify risks and contingency mitigation plans.
• Ensure projects are completed in accordance with the Stryker's quality system
• Establish strategy, tactics, and priorities, imparting a sense of urgency and importance to the team, while using project management tools and techniques to support Stryker business needs
• Lead project team to follow fundamental industry standards, design requirements and test strategies which apply to regulatory requirements
• Lead impact assessment of design changes using product and technical expertise
• Work closely with Project Managers to drive successful project implementation
• Support capital acquisition activity from specifying equipment, contract negotiation, installation, and validation

What You Will Need:

Required Qualifications:

• Bachelor’s degree in Electrical Engineering, Computer Science, Computer Engineering or related discipline
• 6+ years of proven experience leading cross-functional teams to manage project objectives, timelines, and scope

Preferred Qualifications:

• Master’s degree in Engineering
• Experience with medical device integration or equivalent highly regulated industry
• Experience working with cross-functional and outside design partners
• Knowledge and understanding of product development within a regulated quality system, including familiarity with ISO 13485, IEC60601-1 and other related medical device standards 

• $118k - $196k salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.