Senior Quality Manager

Intellectt INC

  • Hayward, CA
  • 17 days ago

    Highlights

    Work with Manufacturing and Project Engineering to implement process improvements and transition projects into production. Benefits: Eligible employees may have access to benefits offered by Intellectt Inc. in accordance with the applicable benefit plans and eligibility requirements.

    Numbers & Facts

    LocationHayward, CA

    Description

    Hello,

    I hope you're doing well.

    My name is Soundarya, and I'm reaching out from Intellectt Inc. regarding an exciting contract opportunity for Sr. Quality Engineer based in Hayward, CA with one of our prestigious clients. I would
    love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at

    soundarya.kondra@intellectt.com

    Job Title: Sr. Quality Engineer
    Location: Hayward, CAWork Arrangement: Onsite
    Experience Level: 5-6 years

    Pay rate: $55-$58/hr on W2

    Job Summary

    We are looking for a Sr. Quality Engineer with experience in medical device quality, process validation, risk management, and computer system validation (CSV). The engineer will support manufacturing processes, product quality, regulatory compliance, and continuous improvement.

    Key Responsibilities

    • Support quality engineering and manufacturing processes from raw materials through finished products.
    • Perform and support process validation and equipment/software validation activities.
    • Execute validation protocols including DQ, IQ, OQ, PQ, and TMV.
    • Develop and maintain risk management documentation for products, processes, and software.
    • Perform root cause analysis, NCR, CAPA, and investigation of quality issues.
    • Analyze process/product data and identify trends or potential quality issues.
    • Support Computer System Validation (CSV), data integrity, and software change-control assessments.
    • Evaluate impacts related to software, hardware, cybersecurity, and data integrity.
    • Develop/review quality procedures and validation documentation in accordance with cGDP/GMP requirements.
    • Work with Manufacturing and Project Engineering to implement process improvements and transition projects into production.
    • Provide guidance on CSV, SDLC, data integrity, and cybersecurity best practices.

    Required Qualifications

    • Bachelor's degree in Engineering or related field.
    • 3 5+ years of Quality Engineering experience, preferably in medical devices.
    • Strong experience with process validation and risk management.
    • Knowledge of CSV/software validation and data integrity.
    • Experience with NCR, CAPA, root cause analysis, and continuous improvement.
    • Strong technical documentation and communication skills.

    Preferred

    • Lean/Six Sigma Green Belt or higher.
    • Experience with regulated medical device/GxP environments.
    • Experience with software validation, SDLC, and cybersecurity assessments.

    Benefits: Eligible employees may have access to benefits offered by Intellectt Inc. in accordance with the applicable benefit plans and eligibility requirements.

    Equal Employment Opportunity: Intellectt Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status, or any other characteristic protected by applicable federal, state, or local law.

    Thanks & Regards,
    Soundarya
    Technical Recruiter
    Intellectt Inc

    Soundarya@intellectt.com


    Direct: 732 204 6899
    Desk number: 732 412 6999 Ext: 247

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