R&D Engineer II

3 weeks ago

Plymouth, United States Abbott Full time

The Opportunity

This position works out of our Plymouth, MN location in the EP division.

In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.

As the R&D Engineer II, you'll have the chance to be part of our Electrophysiology catheter research and development team focused on delivering the future in diagnostic, imaging, and ablation therapy catheters.This role will involve a range of responsibilities including but not limited to 3D CAD models and documentation, design analysis, material research, prototype design, build and testing, design of test fixtures and test method development, manufacturing support and interface with the cross functional product development team.

What You’ll Work On

Design sub-assemblies or processes to meet broad design goals. Establish requirements and specifications using knowledge of component interactions through entire system and downstream impacts of design, material selection and process on system function (aging, sterilization) Use of basic engineering tools such as CAD, tolerance stacks, GD&T Plan, schedule and coordinate project tasks and activities – within overall project schedule goals. Effectively communicate with management and cross functional team members. Conceive and build working prototypes. Run empirical and experimental analysis utilizing various analytical design tools. Work with internal departments and with outside consultants, vendors, machinists, and the medical community. Write protocols and reports with minimal oversight. Make decisions having considered options and using analytical tools, Cpk, tolerance stack, manufacturability, clinical relevance, cross-functional factors, risk benefit, COGS Support bench / animal testing and clinical evaluations. Helps support effective team environment and collaboration. Able to gather, analyze, summarize and present data in a meaningful precise format Establish product requirements and specifications. Develop clinically relevant test models and test methods for design evaluations Create and maintain 3D CAD models, assemblies, and prints Ensure compliance with procedural and documentation requirements of Abbott, FDA , ISO and other regulatory bodies.

Required Qualifications

Bachelor’s degree in Mechanical/Electrical Engineering with 2+ years of engineering experience, mainly in Research & Development in medical device or other highly regulated industry Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization Strong presentation skills to communicate technical challenges across multiple sites Ability to leverage and/or engage others to accomplish projects. Ability to work within a team and as an individual contributor in a fast-paced, changing environment. Ability to work in a highly matrixed and geographically diverse business environment. Ability to prioritizes and meet deadlines in timely manner. Strong organizational skills, as well as attention to detail.

Preferred Qualifications

Masters degree in Mechanical/Electrical Engineering, with 2+ years of relevant experience Experience with a variety of manufacturing processes and design for manufacturability. Experience collaborating with suppliers in the design and procurement of development contracts Experience in designing and testing catheters, or related medical devices. Experience working in a broader enterprise/cross-division business unit Experience in designing electro-mechanical devices.

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