Technology Lead | Embedded Software | Medical Devices

Ipolarity LLC

  • Salt Lake City, UT
  • 21 days ago
  • Remote

    Highlights

    The customer is specifically looking for senior-level engineers capable of operating independently with quality, manufacturing, and operations teams. Please confirm if this would be onsite from day one OR Initial remote for 2-3 months, and then expect the candidate to work from the office OR 100% Remote: Hybrid.

    Numbers & Facts

    LocationSalt Lake City, UT (
    Remote
    )

    Description

    POC Diksha

    Job Details:
    Job title: Senior Quality Analyst (Technology Analyst - US)
    Work Location with Zip code: Salt Lake City, UT 84116 (should be in Utah)
    Duration of the project: 6 Months
    This role requires any travel (Yes/No): NO
    Please confirm if this would be onsite from day one OR Initial remote for 2-3 months, and then expect the candidate to work from the office OR 100% Remote: Hybrid
    Is this a 100% remote role? NO
    Vendor rate range: ####2-65
    Minimum years of experience required: 6-12 yrs
    Would you require the candidates to meet you for an in-person interview? Should be okay with both
    Education Qualification required: Bachelor s / Masters
    Must have skills:
    1. Medical devices
    2. Medical Device Quality Engineering
    3. Manufacturing Quality
    4. Root Cause Analysis and CAPA
    5. SPC / Process Capability Analysis
    6. PFMEA and Control Plans
    7. Plastics Manufacturing and Injection Molding
    8. Assembly and Labeling Processes
    9. FDA and ISO 13485 regulated manufacturing environments
    10. capable of operating independently with quality, manufacturing, and operations teams

    Detailed Job Description:
    1. Medical Device Quality Engineering
    2. Manufacturing Quality
    3. Root Cause Analysis and CAPA
    4. SPC / Process Capability Analysis
    5. PFMEA and Control Plans
    6. Plastics Manufacturing and Injection Molding
    7. Assembly and Labeling Processes
    8. FDA and ISO 13485 regulated manufacturing environments

    The customer is specifically looking for senior-level engineers capable of operating independently with quality, manufacturing, and operations teams.

    Minimum years of experience: 6-12 yrs

    Education: Bachelor s / Masters

    The top 3 responsibilities would expect the Subcon to shoulder and execute:
    FDA and ISO 13485 regulated manufacturing environments
    Root Cause Analysis and CAPA
    Medical Device Quality Engineering

    Project Code: project code for ENGCMD

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