1+ months

Systems Verification Engineer I

Saint Paul, MN

At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.

The Systems Verification Engineer I, working under general supervision, is responsible for providing engineering support to system verification.  Responsibilities include investigating, defining, analyzing, documenting and testing activities associated with the development of larger systems (hardware, software, and catheter).  Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more academic course of study.  Applies engineering and scientific principles to the evaluation and solution of technical problems.  Exercises an appropriate level of technical judgment in planning, organizing, performing and coordinating product development engineering assignments.

Responsibilities Include:

  • Develop new test equipment/methods and perform the validations as required.
  • Performs mechanical dimensioning and tolerance evaluations of components, drawings, and tooling through the use of computer-aided design (CAD; i.e. ProE) techniques
  • Resolves and/or facilitates the resolution of problems including identifying causes to prevent re-occurance
  • Validates equipment and processes as required
  • Work independently and as a team member to plan, write, and execute test cases according to internal processes, FDA regulatory, and ISO standard procedures.
  • Participate in the requirements , hazard analysis, and design reviews for new features.
  • Design new test suites for new features and functionality.
  • Provide verification and validation perspective to R&D’s ongoing product development: requirements, product and test designs, defect reviews, user workflows, and field complaint investigations.

    Required Qualifications:

    • Bachelor of Science degree in biomedical engineering, electrical engineering, mechanical engineering, material science engineering or related engineering field and up to 3 years experience.
    • Demonstrates progressively more responsibility throughout job experience.
    • Broad technical knowledge; expertise in one or more relevant specialties.
    • Experience working in a broader enterprise/cross-division business unit model preferred.
    • Ability to work in a highly matrixed and geographically diverse business environment.
    • Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
    • Ability to leverage and/or engage others to accomplish projects.
    • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
    • Multitasks, prioritizes and meets deadlines in timely manner.
    • Strong organizational and follow-up skills, as well as attention to detail.
    • Ability to travel approximately 10%, including internationally.
    • Ability to maintain regular and predictable attendance.

      Preferred Qualifications:

      • Current industry knowledge of electrophysiology and/or cardiac rhythm management products.
      • Experience with Labview, C++, Perl, and Python programming languages.
      • Experience with automated testing.
      • Experience with robotics, control systems, and/or motor controllers.

        Job Family: Product Development
        Division: CAHF Cardiac Arrhythmias & Heart Failure
        Travel: Not specified
        Medical Surveillance: Not Applicable
        Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)


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Systems Verification Engineer I

Saint Paul, MN

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Saint Paul, MN

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