Product Development Engineer

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  • 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.

Product Development Engineer

  • Specialty:

    Engineering
  • Title:

    Product Development Engineer
    • City:

      Marlborough
    • State:

      MA
    • Zip Code:

      01752
  • Start date:

    06-01-2017
  • Status:

    Closed
  • Assignment Type:

    Direct Hire
  • Job Id:

    42540

Description

Product Development Engineer

 

Responsibilities:

  • Develops new concepts from design to full scale manufacturing and market release. 
  • Investigates and evaluates current technology being utilized
  • Designs and implements new methodologies, materials, machines, processes or products to bring concept to market. This includes essential product and process documentation. 
  • Conducts feasibility studies of the design to determine ability to function as intended.
  • Maintains detailed documentation throughout all phases of research and development.
  • Prepare project plans that specify project phases, tasks, task interdependencies, durations, resource assignments, and costs.
  • Conduct risk analysis for products under development.
  • Coordinates activities with outside suppliers and consultants to ensure the delivery of supplies or services needed to meet scheduled timelines.

Education and Experience:

  • Bachelor's degree in Mechanical or Biomedical Engineering is desired.
  • Minimum of 5 years of medical device product design and development experience is required.

Needed Skills:

  • Demonstrated ability to bring products from concept to market.
  • Ability to interact with client companies in a professional manner.
  • Proficiency in Solidworks
  • Familiarity with FDA QSR and
  • Familiarity with ISO 13485 medical device regulations.
  • Knowledge of probability and statistics.
  • Efficiency in the management of resources.
  • Customer focus with excellent communication skills, written and oral.
  • Depth of knowledge in one or more clinical areas.
  • Depth of knowledge in one or more product areas.
  • In depth of knowledge of FEA
  • Persistence and the ability to adapt to changing schedules
  • Resourcefulness, a drive to succeed, and an entrepreneurial spirit.

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