Systems Engineer

Systems Engineer


Job ID: 9740045

Saint Louis, MO, US

Engineering

Unspecified

Full Time, Temporary

Experienced (Non-Manager)

On-site

Engineering Services

First Shift (Day)

Saint Louis, MO, US

Experienced (Non-Manager)

Full Time, Temporary

Engineering Services

On-site

Engineering

Unspecified

First Shift (Day)

Job details

Systems Engineer | St. Louis, MO
Open Ended Contract (Full Benefits)

 

Candidate will work with the systems team and engineering SMEs as the lead system architect, assisting with requirements finalization, test planning and development, and standard compliance.

As an E2, candidate will be expected to handle multiple assignments at once and show a high capability of operating independently.

  • Perform system architecting with MBSE or similar

  • Read and understand applicable industry standards and government regulations

  • Perform risk analysis and design mitigations

  • Decompose complicated systems into implementable subsystems

  • Write requirements for subsystems of medical devices

  • Design interfaces between subsystems

  • Manage integration of the systems into the whole

  • Create plans and protocols to ensure testing is complete

  • Design automated test methods for reliability & life testing of subsystems likely to wear

  • Maintain V&V plan and coordinate with test engineers to get test executed

 
Internal customers:  R&D SMEs, Project Manager, Manufacturing Engineers, QA, Regulatory, Purchasing, & Supplier Quality
External customers:  Potential technical interaction with suppliers.
Minimum requirements:  BS in Engineering (Systems, Biomedical, Electrical, Mechanical), related physical science, or equivalent experience, & 3-7 years experience as an engineer.  Excellent communications & organizational skills.  High degree of self-motivation and direction.

Preferred requirements:  Experience with a medical device company writing or maintaining requirements, reports, & test plans.  Training and experience with MBSE or similar methods.  Familiarity with relevant regulations & industry standards (FDA, MDR, IEC, & ISO).  Experience using our tool chain (MS Office, ReqPro, ClearQuest, Aras PLM)

9740045

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