We anticipate the application window for this opening will close on - 1 Aug 2025

 

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

Provide development support of released production heart valve repair and replacement products that meet application, business, customer and regulatory requirements. Based on input from business partners, prepare schedules and proposals for modifications to designs that meet all Quality and customer requirements. Function effectively as a technical contributor for projects in multi-functional team environment. Collaborate with Manufacturing and Quality colleagues to ensure designs are capable of being manufactured consistently and cost effectively. Document design in accordance with applicable Product Development Protocol, Quality and Regulatory requirements. Prepare regulatory submission-ready documentation for the FDA and other regulatory bodies. Support multiple projects within the surgical valve Sustaining/Released Product Engineering group. Provide work direction and training to other engineers and technicians.

Careers That Change Lives  
 
At Medtronic, we push the limits of what technology can do to make tomorrow better than yesterday and that makes it an exciting and rewarding place to work. We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations. 

A Day in the Life 

Provide development support of released production heart valve replacement and repair products that meet application, business, customer and regulatory requirements.  Based on input from business partners, prepare schedules and proposals for modifications to designs that meet all Quality and customer requirements.  Function effectively as a technical contributor for projects in multi-functional team environment.  Collaborate with Manufacturing and Quality colleagues to ensure designs are capable of being manufactured consistently and cost effectively.  Document design in accordance with applicable Product Development Protocol, Quality and Regulatory requirements.  Prepare regulatory submission-ready documentation for the FDA and other regulatory bodies.  Support multiple projects within the surgical valve Sustaining/Released Product Engineering group.  Provide work direction and training to other engineers and technicians. 

 

Responsibilities may include the following and other duties may be assigned: 

• Contribute to the design, development and support of existing and modified production heart valve products in a regulated environment. 

• Support sustaining engineering programs for new and existing products to ensure sustainable and stable operations of production.  Identify areas that require additional investigation. 

• Support manufacturing and quality groups for improvements to existing products in the areas of quality enhancement, product cost and product performance. 

• Analyze and recommend solutions to product issues as a result of product complaints, Manufacturing and/or Quality issues. 

• Review and approve document change orders for design, materials, and process documentation. 

• Responsible for production support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; minor redesign of devices and masks; analysis of customer returns; supplier related engineering changes and optimizing device production relative to cost constraints. 

• Participate in the specification an