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Principal R&D Systems Engineer - Electrophysiology

Lead the design and validation of electrophysiology ablation catheter systems
Arden Hills, Minnesota, United States
Senior
$99,100 – 188,300 USD / year
19 hours agoBe an early applicant
Boston Scientific

Boston Scientific

A global medical device manufacturer specializing in products for various interventional medical specialties, including cardiac, vascular, and urological conditions.

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Principal R&D Systems Engineer - Electrophysiology

Work mode: Onsite

Onsite Location(s): Arden Hills, MN, US, 55112

About the role:

The Ablation Catheter Development Team is growing and has an exciting opportunity for a Principal Systems Engineer role supporting Electrophysiology product development within the Cardiology division. Electrophysiology is an exciting growth driver for BSC. With the acquisition of FARAPULSE Inc., Boston Scientific will strengthen its leadership in Personalized EP Solutions, with a strong focus in Atrial Fibrillation.

The principal engineer role will be a key team member in providing systems engineering support in the creation and development of new electrophysiology ablation catheter technologies and the integration of those products into the larger system. As Principal Engineer, you will support new product development team solutions to multi-faceted customer issues, requiring applied in-depth problem-solving competencies.

You will be a part of a high-performance team responsible for the design, implementation, and test of medical devices within our electrophysiology pulsed field ablation device portfolio. This critical role will be a part of best-in-class development practices and rigorous, holistic product design in coordination with internal and external partners.

Key Responsibilities:

  • Researches, develops, designs, and evaluates: mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment.
  • Develops solutions to diverse engineering problems of high complexity which require the regular use of ingenuity and creativity. Leverages internal/external partners as necessary to achieve project objectives.
  • Drives technical aspects of complex device development including requirements, design, implementation, test, integration, transfer to manufacturing, and verification/validation.
  • Translates user needs to create technical requirements aligned to design through the development cycle toward successful execution of usability and validation plans toward regulatory submission and approval
  • Understands, evaluates, and shares clinical practice and expectation that drive design and test to improve product integration and usability
  • Solves system problems by analyzing the situation and recommending corrective or alternative actions. Leads technical teams through problem solving. Facilitates crisp decision making around key technical issues.
  • Plans and organizes project assignments of substantial variety and complexity. Directs support personnel and project activities.
  • Ensure quality system compliance for medical device development, champion continuous improvement, and adopt best practices.
  • Participates in the development of others by facilitating training and providing feedback and guidance.
  • Creates a strong team culture around high expectations and high performance
  • Writes and submits intellectual property (patents).
  • Maintains detailed documentation throughout all phases of research and development.
  • Provides clear communication to stakeholders at key technical updates.

Required qualifications:

  • BS degree in Mechanical, Electrical, Biomedical, or Systems Engineering
  • Required minimum years of work experience (primarily in medical device or related field): 7+ Years with BS, 5+ Years with MS
  • Experience with Design/Technical skills in complex electromechanical systems with the ability to demonstrate a good understanding of the fundamentals of Design.
  • Experience managing technical aspects of projects as a member of a cross-functional core team
  • Demonstrated strong cross-functional collaboration, influence without authority, and project/task management enabling highly effective teams
  • Experience working with Electrophysiology and/or Class II or Class III Medical Device products.
  • Experience working within a quality system, IEC and ISO standards relevant to medical device lifecycle and risk management (i.e., ISO 13485).
  • Passion for understanding and solving problems for end users
  • Strong written and oral communication skills

Preferred qualifications:

  • Proven self-starter who runs towards critical issues, ambiguous requirements, or loosely defined challenges with a demonstrated ability to rally teams to achieve business results.
  • Demonstrated product development leadership and communication skills.
  • Demonstrated ability to provide technical leadership on a large-scale development program
  • Ability to draw conclusions and make recommendations based on technical inputs from multiple and varied sources.
  • Systems engineering mindset, able to articulate customer unmet needs and translate into holistic technical solutions.
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Principal R&D Systems Engineer - Electrophysiology
Arden Hills, Minnesota, United States
$99,100 – 188,300 USD / year
Engineering
About Boston Scientific
A global medical device manufacturer specializing in products for various interventional medical specialties, including cardiac, vascular, and urological conditions.