Staff R&D Engineer-Predictive Engineering & Validation – Electrophysiology

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

Job description

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

• Career development with an international company where you can grow the career you dream of.

• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

• An excellent retirement savings plan with a high employer contribution

• Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

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

Leading an active lifestyle is important to the many people we serve. In Abbott's Electrophysiology (EP) division, we're advancing the treatment of heart rhythm disorders through breakthrough medical technologies, allowing people to restore their health and get on with their lives.

What You’ll Work On

As a Staff R&D Engineer, Predictive Engineering & Validation, you will provide technical leadership for the development and execution of advanced bench testing strategies that support the Electrophysiology product portfolio. This role will establish and drive a vision for expanding bench testing capabilities to generate high-quality, decision-driving data that accelerates product development and complements preclinical studies.

You will work across engineering, clinical, systems, and regulatory functions to develop innovative test methods, models, and evaluation frameworks that increase confidence in design decisions, optimize development costs, and improve development speed. The successful candidate will be recognized as a technical expert and strategic leader, influencing technology development across multiple projects.

Primary Responsibilities

• Lead the strategy, development, and implementation of advanced bench testing capabilities supporting electrophysiology therapies and technologies.

• Establish technical roadmaps that increase the use of bench-generated data to inform product design, performance characterization, and development decisions.

• Develop innovative test methods, simulated use models, and experimental platforms that replicate clinically relevant conditions.

• Partner with R&D, Clinical, Systems Engineering, Regulatory, Quality, and Product Development teams to align testing strategies with project objectives.

• Serve as a subject matter expert for bench testing methodologies, data interpretation, and study design.

• Lead complex investigations and data-driven analyses supporting technology development, risk reduction, and design optimization.

• Define requirements for new laboratory equipment, testing infrastructure, and capability investments.

• Mentor engineers and scientists in experimental design, data analysis, and best practices for bench testing.

• Present technical recommendations and strategic proposals to functional leadership and project teams.

• Support development of verification and validation strategies and associated regulatory documentation.

• Identify opportunities to improve efficiency, reduce development costs, and accelerate project timelines through innovative testing approaches.

• Ensure compliance with FDA regulations, ISO standards, company procedures, and quality system requirements.

Required Qualifications

• Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemical Engineering, or related technical discipline.

• 8+ years of medical device product development, testing, research, or engineering experience.

• Demonstrated experience leading complex technical initiatives and influencing cross-functional teams.

• Strong understanding of experimental design, engineering fundamentals, and data-driven decision-making.

• Experience developing and executing laboratory, bench, or preclinical testing methodologies.

• Strong analytical and problem-solving skills with the ability to evaluate complex technical challenges.

• Excellent written, verbal, and presentation communication skills.

• Ability to effectively influence stakeholders and drive technical decisions across multiple organizations.

Preferred Qualifications

• Strong preference for candidates with demonstrated expertise in Irreversible Electroporation (IRE)/ Pulsed Field Ablation (PFA) technology platforms, including electroporation physics, tissue response, energy delivery systems, catheter-based therapies, and cross-functional product development activities.

• Advanced degree (M.S. or Ph.D.) in Engineering, Biomedical Engineering, or related field.

• Experience in electrophysiology, cardiovascular medical devices, catheter-based therapies, or related technologies.

• Experience developing physiologically relevant bench models and simulation systems.

• Knowledge of verification and validation methodologies in regulated medical device environments.

• Experience with signal acquisition, data analysis, statistics, and modeling techniques.

• Experience leading laboratory capability development, test infrastructure improvements, or technology platforms.

• Demonstrated success mentoring engineers and serving as a technical leader across multiple projects.

• Knowledge of FDA regulations, ISO 13485, risk management processes, and design control requirements.

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.

The base pay for this position is $99,300.00 – $198,700.00

In specific locations, the pay range may vary from the range posted.

Job family Product Development

Divisione EP Electrophysiology

Sede di lavoro United States > Minnesota > Plymouth : 5050 Nathan Lane N

Sedi di lavoro ulteriori

Turni Standard

Viaggiare Yes, 10 % of the Time

Controllo medico No

Attività lavorative significative Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf