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Systems Engineer Iii

  • ... Posted on: Sep 13, 2024
  • ... Intellectt INC
  • ... Saint Louis, Missouri
  • ... Salary: Not Available
  • ... CTC

Systems Engineer Iii   

Job Title :

Systems Engineer Iii

Job Type :

CTC

Job Location :

Saint Louis Missouri United States

Remote :

No

Jobcon Logo Job Description :

Systems Engineer III

Location: St. Louis, MO - Onsite
Duration: 6 months

Role Overview:

We seek a Systems Engineer III to support the development of a new ophthalmic surgical system. You will work with regulatory, quality, and R&D teams to finalize requirements, perform risk analysis, and prepare documentation.

Key Responsibilities:
  • Interpret industry standards and regulations.
  • Develop testable requirements and perform risk analysis.
  • Assist in test development and resolve integration issues.
  • Use Aras PLM for design traceability.
Qualifications:
  • Education: BS in Engineering (Systems, Biomedical, Electrical, Mechanical)
  • Experience: 7+ years with complex electro-mechanical systems and regulatory requirements
  • Skills: Risk analysis, requirement management, verification planning, and excellent communication
Preferred:
  • Experience with surgical medical devices
  • Knowledge of FDA, MDR, ISO, and other relevant standards
  • Experience with Aras PLM and medical device labeling

    Sonali Kumari Roy | Talent Acquisition Specialist

    Intellectt INC
    phone-icon 732 979 2751 Ext: 580
    phone-icon
    phone-icon 517 Route 1 South, Suite 1115 Iselin, NJ 08830,

    If you prefer not to receive further communications from us, kindly click :

Jobcon Logo Position Details

Posted:

Sep 13, 2024

Employment:

CTC

Salary:

Not Available

Snaprecruit ID:

SD-CIE-c5d9b6141804ab8791685751d2636a2b5a5aa056b520584c5aa3ce60264fc65c

City:

Saint Louis

Job Origin:

CIEPAL_ORGANIC_FEED

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Systems Engineer III

Location: St. Louis, MO - Onsite
Duration: 6 months

Role Overview:

We seek a Systems Engineer III to support the development of a new ophthalmic surgical system. You will work with regulatory, quality, and R&D teams to finalize requirements, perform risk analysis, and prepare documentation.

Key Responsibilities:
  • Interpret industry standards and regulations.
  • Develop testable requirements and perform risk analysis.
  • Assist in test development and resolve integration issues.
  • Use Aras PLM for design traceability.
Qualifications:
  • Education: BS in Engineering (Systems, Biomedical, Electrical, Mechanical)
  • Experience: 7+ years with complex electro-mechanical systems and regulatory requirements
  • Skills: Risk analysis, requirement management, verification planning, and excellent communication
Preferred:
  • Experience with surgical medical devices
  • Knowledge of FDA, MDR, ISO, and other relevant standards
  • Experience with Aras PLM and medical device labeling

    Sonali Kumari Roy | Talent Acquisition Specialist

    Intellectt INC
    phone-icon 732 979 2751 Ext: 580
    phone-icon
    phone-icon 517 Route 1 South, Suite 1115 Iselin, NJ 08830,

    If you prefer not to receive further communications from us, kindly click :

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