Quality Assurance

  • #3266834
    Sigmagraft, Inc 63.***.193.161 496

    Sigmagraft, Inc.

    Fullerton, CA, USA

    Job posting expires at 2018-11-30

    ESSENTIAL JOB DUTIES
    • Perform raw material incoming inspections including and packaging material checks to ensure requirements are met— document and communicate results.
    • Perform Daily Operating Inspections as needed to assure compliance with GMPs requirements.
    • This position is responsible for day-to-day QA sampling collections that includes (but is not limited to) all sampling required for company bioburden control programs.
    • This position will maintain accurate collection and record keeping of all sampling information, audit results and other project information.
    • This position also performs scheduled facility audits and all documentation pertaining to those audits.
    • Report and follow-up on quality concerns.
    • Assists in customer concern investigations, including evaluation of retains, returned product, and raw materials to help determine concern validity and investigate root cause.
    • Document establishment, review and approval
    Required Qualifications
    • Bachelor’s degree
    • Relevant work experience in a medical device, pharmaceutical, or food processing industry field.
    • Experience with FDA requirements, knowledge of regulations such as GMP, ISO 13485 and other international regulatory requirements preferred, but not required.
    • Previous experience with Quality Management System development, implementation, and monitoring.
    • Knowledge of quality systems, technical writing and training skills is preferred.
    • A strong working knowledge of Microsoft Excel, Microsoft Word, Microsoft PowerPoint and Microsoft Outlook.
    • Excellent communication, organizational, analytical and interpersonal skills.
    • Must be a person of passion and integrity who has the drive to excel and deliver exceptional results.

    Highly qualified candidates will also possess:
    • Previous experience working with the ISO 13485 quality management system
    • Previous experience with FDA cGMP
    • Experience with ISO and/or FDA audits
    • The ability to solve practical problems or issues
    • The ability to communicate and interact with coworkers in a positive manor
    • The ability to work swiftly and accurately
    • The ability to recognize and solve practical problems or issues