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    Medical Device Quality Engineer - Westborough, United States - Talent Groups

    Talent Groups
    Talent Groups Westborough, United States

    2 weeks ago

    Default job background
    Description
    • 5 years of experience in Quality Assurance/Quality Engineering within medical device or pharmaceutical industries.
    • Proficient understanding or demonstrated aptitude for understanding Medical Device Quality Management System (QMS) requirements and regulatory standards such as FDA CFR and ISO 13485.
    • Familiarity with product development lifecycles, including design change and document change control.
    • Competence in process verification and validation methodologies.
    • Proficient in using word processing, spreadsheet, and presentation software.
    • Knowledgeable about continuous quality/process improvement tools.
    • Strong understanding of regulatory compliance within the medical device/pharmaceutical sectors.
    • Ability to analyze and interpret quality data to drive improvements.
    • Excellent communication and interpersonal skills.

    Desired Job Titles: Senior Quality Engineer, Quality Assurance Engineer, Medical Device Quality Specialist, Regulatory Compliance Engineer, Quality Control Engineer, Validation Engineer, Process Improvement Engineer, Supplier Quality Engineer, Manufacturing Quality Engineer


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