28d ago

Senior Preclinical Interventionalist

United States - Minnesota - Plymouthsenior
Other
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Quick Summary

Overview

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,

Technical Tools
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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.

     

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.

This position works out of our Plymouth, MN division in the EP division in R&D.

As the Senior Preclinical Interventionalist, you will support our EP product development team focused on delivering the future in diagnostic, imaging, and ablation therapy catheters and EP capital equipment.

This role will involve a range of responsibilities including but not limited to

preclinical study execution, requirement development, testing and data analysis, validation testing, and serving as a consultant on clinical workflows and risk evaluation documentation.

  • Serve as a subject matter expert for appropriate use of EP products during preclinical study execution.
  • Train co-workers and physician customers in the preclinical environment.
  • Provide feedback and insight on clinical workflows and clinical use of EP products to product teams Support development of risk management documentation.
  • Design, conduct/supervise, and support bench and preclinical studies for product concept feasibility and formal regulatory submission.
  • Plan, coordinate, and conduct empirical and experimental analysis.
  • Organize and analyze data from experiments or design builds and write reports on results.
  • Conduct research and prepare research tasks.
  • Document work suitable for technical papers and patents.
  • Participate in project design reviews and project planning
  • Track performance against plan. Develop plan in conjunction with technical supervisor.
  • Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
  • Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
  • Perform other related duties and responsibilities, on occasion, as assigned.

Requirements

~1 min read
  • Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, biological sciences, medical/clinical science or equivalent experience.
  • 5+ years' experience as a preclinical interventionalist, experience with cardiac electrophysiology devices preferred.
  • Experience working within a team and as an individual contributor in a fast-paced, changing environment.
  • Strong verbal and written communications with ability to effectively communicate at multiple levels of the organization.
  • Strong organizational and follow-up skills, as well as attention to detail.
  • Strong technical leadership skills including the ability to coach and mentor less experienced employees.
  • Ability to work in a highly matrixed and geographically diverse business environment.
  • Ability to leverage and/or engage others to accomplish projects.
  • Ability to multitask, prioritize and meet deadlines in timely manner.
  • Ability to travel 10 — 25%.

  • Experience working as a study director in a preclinical setting, preferably with cardiac electrophysiology devices.
  • Experience working in a broader enterprise/cross-division business unit model preferred.
  • Medical device industry experience Ability to plan, execute, analyze, and document individual scientific studies.

Apply Now

What We Offer

~1 min read
$78,000.00 – $156,000.00

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

     

Product Development

     

EP Electrophysiology

        

United States > Minnesota > Plymouth : 5050 Nathan Lane N

     

     

Standard

     

Yes, 25 % of the Time

     

No

     

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours 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

Location & Eligibility

Where is the job
United States - Minnesota - Plymouth
On-site at the office
Who can apply
Same as job location

About this job

Posted
28 days ago
Employer
has 4,356 open jobs on Jobera in 26 countries.

Listing Details

Posted
September 17, 2026
First seen
September 28, 2026
Last seen
October 15, 2026

Posting Health

Days active
16
Repost count
0
Trust Level
19%
Scored at
October 15, 2026

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Senior Preclinical Interventionalist