Senior Preclinical Interventionalist

Job ID: 31162113Posted: Posted 2 Days AgoStart Date: 2026-09-17Location: United States - Minnesota - Plymouth, United States of AmericaTime Type: Full timeAbbott 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 AbbottAt 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 contributionTuition 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 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. What You’ll Work OnServe 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 planningTrack 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.Required QualificationsBachelor'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%.Preferred QualificationsExperience 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 NowLearn more about our health and wellness benefits, which provide the security to help you and your family live full lives: 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 , on Facebook at , and on Twitter @AbbottNews.The base pay for this position is $78,000.00 – $156,000.00In specific locations, the pay range may vary from the range posted.JOB FAMILY:Product DevelopmentDIVISION:EP ElectrophysiologyLOCATION:United States > Minnesota > Plymouth : 5050 Nathan Lane NADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 25 % of the TimeMEDICAL SURVEILLANCE:NoSIGNIFICANT WORK ACTIVITIES: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: is the Law link - Espanol: