Sr Product Development Engineer

Sorry, this particular job is closed. But feel free to fill out a General Application

Search Jobs

General Apply

  • As an Equal Employment Opportunity Employer, DAVIS has reporting requirements which require us to invite employees to voluntarily self-identify their race/ethnicity. Submission of this information is voluntary and refusal to provided it will not subject you to any adverse treatment. The information obtained will be kept confidential.
  • By applying to this position and providing my contact information, I give The DAVIS Companies permission to provide me with email communications and information.

Sr Product Development Engineer

  • Specialty:

    Engineering
  • Title:

    Sr Product Development Engineer
    • City:

      Minneapolis
    • State:

      MN
    • Zip Code:

      55428
  • Start date:

    11-21-2017
  • Status:

    Closed
  • Assignment Type:

    Contract To Hire
  • Job Id:

    44012

Description

The DAVIS Companies has partnered with a global leader in the medical device industry by securing a Sr Product Development Engineer to join their team. 

This individual will design and develop medical devices from concept through market introduction. The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, entrepreneurial environment.

Responsibilities of Sr Product Development Engineer: 

• Design and develop medical instruments (disposable and reusable), catheters, implants, and/or packaging, from concept through market introduction. Ensure that designs meet performance specifications, regulatory and manufacturing requirements.
• Manage product development projects. Prepare project plans that specify project phases, tasks, task interdependencies, durations, resource assignments, and costs. Proactively communicate task assignments to responsible individuals, and ensure that tasks are completed within the planned time. Track projects to project plans. Proactively report project status to personnel and to the project’s client company.
• Utilize SolidWorks to develop detailed 3-D CAD models and drawings of medical instruments (disposable and reusable), catheters, implants, and/or packaging. Includes component, subassembly, and top-level drawings.
• Generate innovative concepts for new medical device designs to satisfy clinical requirements. Lead and participate in concept generation activities, including brainstorming sessions. Refine, rate, rank and/or otherwise assess concepts.
• Interact with client companies in a professional manner. Proactively communicate with client companies to ensure an ongoing two-way exchange of information.
• Generate project timing and expense estimates and prepare project proposals for client companies.
• Maintain Design History Files (DHFs) per company procedure. Ensure that DHFs are accurate, complete and well organized.
• Conduct risk analysis for products under development. Conduct and document Failure Mode and Effects Analysis per company procedure.
• Perform tolerance analysis of components and assemblies to ensure proper fit and function.
• Conduct product verification and validation testing to demonstrate product safety and efficacy. Determine what testing is required to satisfy product requirements, to investigate potential failure modes, and to otherwise address the project design inputs. Develop protocols, plan testing, and perform or monitor testing. Utilize statistical methods as required to plan testing and to analyze test results. Write test reports which draw conclusions from the results.
• Produce prototype devices for testing, and for evaluation by client companies. Work with internal and/or external resources to produce prototype device components. Assemble and/or evaluate prototype devices.
• Conduct Design Reviews as specified in project plans, and in accordance with company procedure.
• Prepare documentation release packages, including detail drawings, bills of material, and/or procedures. Approve Document Change Orders (DCOs) and obtain approvals from others as required.
• Participate in Material Review Board activities. Make decisions regarding product and material discrepancies and initiate appropriate action to prevent subsequent problems or discrepancies.
• Date, sign and have witnessed all documents that may establish inventorship dates.
• 10-20% travel 

Required Experience of Sr Product Development Engineer: 

• Bachelor's degree in Mechanical or Biomedical Engineering is required. Master’s degree in engineering, management or business is desired.
• Minimum of 5 years of medical device product design and development experience is required.
• Demonstrated ability to bring products from concept to market.
• SolidWorks 3D CAD proficiency.
• Familiarity with FDA QSR and ISO 13485 medical device regulations.
• Knowledge of probability and statistics.
• Depth of knowledge in one or more clinical areas; interventional cardiology is desired.
• Depth of knowledge in one or more product areas; catheters is desired.
• Depth of knowledge in one or more technical areas, for example finite element analysis.
• Flexibility, persistence, resourcefulness, a drive to succeed, and an entrepreneurial spirit.

More Info

Contact

Similar Positions

Loading...