Sr R&D Engineer (Onsite)

Overview When you join the team at Cordis, you become part of an inspiring mission to save lives, impacting millions of people and broadening access to life-saving cardiovascular and endovascular technology. As a global leader for over 60 years, we are dedicated to being the heart of innovation to transform cardiovascular care. At Cordis, we're teammates, not just employees. We embrace an empowered and one-team culture where teammates are inspired to unleash their full potential. With diverse teams on a global scale, we believe the richness of our experiences and backgrounds enhances the careers of our teammates, the service to our customers, and ultimately, the lives of our patients. If you love a challenge and are ready to have a direct, transformative and positive impact on the lives of millions, then Cordis is just the place for you. We are the people behind the people who keep saving lives. Responsibilities Cordis Corporation designs, manufactures, and commercializes medical devices uses to treat coronary artery disease and peripheral artery disease. Examples of such devices include systems for gaining access to the vasculature, angioplasty balloon catheters, stents and stent delivery systems, and access closure devices. As an R D engineer you will work in the design, development, and testing of Cardiovascular and Vascular Medical Devices. Engineers at Cordis work to solve complex problems to ensure devices meet user needs, and that they are safe and effective for their indicated uses. Responsibilities

• Applies comprehensive medical device engineering knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects.
• May contribute to the development of policies and procedures.
• Works on complex projects of medium scope.
• Develops technical solutions to a wide range of difficult problems. Solutions are innovative and consistent with organization objectives.
• Completes work independently, receives general guidance on new projects.
• Accountable for design reviews as applicable ensuring design solutions are documented, evaluated against design input, and tested properly.
• Works on the design of devices and components assigned as an individual technical contributor, but capable of acting as a project leader as needed.
• Works closely with manufacturing engineers on process development for mass production of medical devices.
• Develops and monitors work schedule to ensure on-time completion of design activities assigned.
• Collaborate with cross-functional teams, including product management, regulatory affairs, quality assurance, and manufacturing, to define and execute product development strategies.

Qualifications Required Qualifications - Requires Engineering Bachelors Degree plus 5+ years of relevant experience. - A minimum of 5+ years of experience (depending on qualifications) in medical device research and development, with a focus on supporting complex projects and driving technical excellence.