Systems Test Engineer II — Medical Device (Onsite — Valencia,CA) Contract

Pharmavise Corporation

  • Valencia, California
  • 30+ days ago
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    Skills

    • Analysis Skillsunmatched
    • Change Requests/Ordersunmatched
    • Computer Firmwareunmatched
    • Computer Scienceunmatched
    • Continuous Improvementunmatched
    • Cross-Functionalunmatched
    • Debugging Skillsunmatched
    • Desktop PCunmatched
    • Electrical Engineeringunmatched
    • Financial Managementunmatched
    • Fortune 500 Customersunmatched
    • Functional Analysisunmatched
    • GitHubunmatched
    • HRIS/HRMSunmatched
    • Manufacturing Process Engineeringunmatched
    • Materials Managementunmatched
    • Medical Equipmentunmatched
    • Operating Systemsunmatched
    • Procedure Developmentunmatched
    • Process Improvementunmatched
    • Programming Languagesunmatched
    • Programming Methodologiesunmatched
    • Python Programming/Scripting Languageunmatched
    • Quality Managementunmatched
    • Quality Metricsunmatched
    • Record Keepingunmatched
    • Reporting Skillsunmatched
    • Requirements Managementunmatched
    • Research & Development (R&D)unmatched
    • Software Administrationunmatched
    • Software Designunmatched
    • Software Developmentunmatched
    • Software Engineeringunmatched
    • Software Testingunmatched
    • System Testunmatched
    • System Validationunmatched
    • Systems Engineeringunmatched
    • Test Plan/Scheduleunmatched
    • Testingunmatched

    Description

    Our F500 Medical Device client has an exciting opportunity for a Systems Test Engineer.

    Job Summary:

    Develops software systems, applications, firmware, and/or provides software systems testing and validation in support of R&D and/or Manufacturing Process Engineering. Responsible for analyzing, designing, programming, debugging, and modification of local, network/internet-related computer programs for commercial or end user applications (i.e. materials management, financial management, HRIS, or desktop applications products). May interface with users to define system requirements and/or necessary modifications. Responsible for developing, applying and maintaining quality standards for software products.

    Responsibilities:
    1. Designs, develops, debugs, modifies, tests software programs by using current programming languages, methodologies and technologies.

    2. Documents software development and/or test development by writing documents, reports, memos, change requests. Methods used are determined by approved procedures and standards.

    3. Tracks software development effort by creating and maintaining records in the approved tracking management tool.

    4. Analyzes, evaluates, verifies requirements, software and systems by using software engineering practices.

    5. Investigates, research, selects software designs, operating systems and/or practices.

    6. Continuously improves process and work methodologies by interfacing with peers/cross-functional groups and analyzing activities to improve workflow and work processes.

    Quality Systems Duties and Responsibilities:

    Build Quality into all aspects of their work by maintaining compliance to all quality requirements.


    Minimum Qualifications

    ·        2 - 4 Years with BS (in Computer science or Electrical Engineering) 1 - 2 Years with MS

    ·        Must have 4-5 years' experience in System Test verification, Python expertise, Github/Bitbucket exp

    Preferred Qualifications

    ·        Medical Device industry experience

    Other Details:

    Schedule: 08:00:AM - 04:30:PM

    Work Setup: Onsite in Valencia, CA

    Contract Length: 6 Months (2/9/2026 – 08/7/2026)



    Numbers & Facts

    LocationValencia, California
    Websitehttp://www.pharmavise.com

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