Sr Systems 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.
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Sr Systems Engineer

  • Specialty:

    Engineering
  • Title:

    Sr Systems Engineer
    • City:

      Bedford
    • State:

      MA
    • Zip Code:

      01730
  • Start date:

    07-27-2018
  • Status:

    Closed
  • Assignment Type:

    Direct Hire
  • Job Id:

    46008

Description

We are looking for a Sr Systems Engineer to join our client in Bedford, MA on a direct hire basis. 

The Sr. Systems Engineer will lead projects and work collaboratively with Engineers, Scientists, Quality, Management, and external partners/consultants for all stages of product development.  You will create plans, requirements, designs/models, prototypes, risk analyses, design output, processes, protocols, reports, traceability analyses, and test fixtures/utilities. You will perform analyses, conduct experiments, develop designs, conduct design reviews, and implement/integrate/verify designs.

Responsibilities

  • Planning of projects/tasks throughout the product lifecycle, concept through commercialization.
  • Development and design verification of complex IVD device and disposables including HW, optics, magnetics, and fluidics.
  • Lead development and design transfer activities with external development and manufacturing, partners and consultants.
  • Oversee product certification, e.g. CE, IEC 61000, IEC 61010, & IEC 61326.
  • Ensure compliance with the Quality Management System for 21 CFR 820 & ISO 13485.
  • Develop appropriate processes and procedures.
  • Develop/operate test software, e.g. LabVIEW, python, and custom internal utilities.
  • Help set up clinical study sites and prepare 510(k) regulatory submissions.

Required Education/Experience/Characteristics

  • BS in electrical, mechanical, or biomedical engineering. MS preferred.
  • 7-10 years of systems engineering experience in a medical device/IVD company.
  • Hands-on experience with programmable electro-mechanical instrument development.
  • Experience creating design control documents for the DHF including plans, requirements, risk management, protocols, reports, design output, design/phase reviews, and traceability analyses.
  • Experience in bringing products to market including FDA clearance/approval.
  • Self-motivated and able to prioritize and organize time effectively.
  • Excellent record-keeping, written and oral skills.
  • Highly organized, pays attention to detail, and completes assigned tasks on time.
  • Proactively communicates with supervisor and team.
  • Effectively communicates across internal & external teams to ensure all requirements are met.
     

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