Senior Preclinical Interventionalist

Abbott; Iowa (LA); On-site; USD 78,000 - 156,000; Full time

Job summary

Abbott in Plymouth, MN seeks a Senior Preclinical Interventionalist to advance EP catheter and capital equipment development. You will conduct preclinical studies, assist in requirement development, testing, data analysis, and contribute to regulatory documentation.

The role requires a Bachelor’s degree in engineering/sciences, 5+ years in preclinical interventionalism, and strong communication. Travel up to 25% and collaboration across teams are expected.

Qualifications

• Bachelor’s degree in engineering or sciences and relevant experience.
• 5+ years’ experience as a preclinical interventionalist, EP device experience preferred.
• Strong verbal and written communications across multiple levels.

Responsibilities

• Serve as SME for appropriate use of EP products during preclinical study execution.
• Train coworkers and physician customers in the preclinical environment.
• Provide feedback on clinical workflows and assist risk management documentation.
• Design, conduct, and oversee bench and preclinical studies for concept feasibility and regulatory submission.
• Plan and perform empirical analyses and data interpretation.
• Organize data, write reports, and document work for papers and patents.
• Participate in project design reviews and planning; track progress against plan.
• Ensure FDA and regulatory compliance and maintain cross-functional collaboration.

Skills

5+ years’ experience as preclinical

Cardiac electrophysiology devices

Education

Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, biological sciences, medical/clinical science or equivalent

Job description

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 forfree medical coverage in ourHealth Investment Plan (HIP) PPOmedical 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 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 On

• 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.

Required Qualifications

• 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%.

Preferred Qualifications

• 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.

The base pay for this position is

$78,000.00 – $156,000.00

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

JOB FAMILY:

Product Development

DIVISION:

EP Electrophysiology

LOCATION:

United States > Minnesota > Plymouth : 5050 Nathan Lane N

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Yes, 25 % of the Time

MEDICAL SURVEILLANCE:

No

SIGNIFICANT 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: http://webstorage.abbott.com/common/External/EEO_English.pdf

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