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About the role:
As Senior 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 disposable medical devices within our electrophysiology pulsed field ablation single use 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 using ingenuity and creativity. Leverages internal/external partners as necessary to achieve project objectives.
Drives technical project tasks within single use device development including requirements, design, implementation, test, integration, transfer to manufacturing, and verification/validation.
Solves system problems by analyzing the situation and recommending corrective or alternative actions. Leads technical workstreams through problem solving. Facilitates crisp decision making around key technical issues.
Independently plans and organizes project tasks with showing the ability to prioritize tasks, execute, and direct others
Ensure quality system compliance for medical device development, champion continuous improvement, and adopt best practices.
Participates in the development of others by providing coaching and guidance.
Creates a strong team culture around high expectations and high performance
Participates in writing and submission of intellectual property (patents).
Maintains detailed documentation throughout all phases of research and development.
Provides clear communication to Technical Leaders at key technical updates.
Required qualifications:
BS degree in Mechanical Engineering
Required minimum years of work experience (primarily in medical device or related field): 5+ Years with BS, 3+ Years with MS
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
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.
Experience with electrophysiology and/or Class II or Class III Medical Device product development experience.
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.
Understanding of working within a quality system, IEC and ISO standards relevant to medical device lifecycle and risk management (i.e., ISO 13485).
Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
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