Postmarket Surveillance Specialist III - Salt Lake City, United States - bioMerieux SA Career Site - MULTI-LINGUAL

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    Description

    Description

    Essential Job Duties and Responsibilities

    • Perform all work in compliance with company policy and within the guidelines of BioFire's Quality System.
    • Follows laws and regulations applicable to Postmarket Surveillance.
    • Conducts, reviews and closes complaint investigations within the Complaint Investigation software tool according to processes.
    • Conducts and reviews escalated complaints for potential reportable events.
    • Coordinates with regulatory affairs to complete reportable event documentation.
    • Review trend charts and perform data analysis.
    • Work with experts from other departments during investigation process.
    • Review complaints for CAPA.
    • Conduct product literature review and work with other departments to address product performance in the field.
    • Perform weekly statistical performance review to monitor manufactured product.
    • Ensure trends are reported to the Postmarket surveillance management.
    • Ensure PSS I & II are adequately trained and prepared to handle complaints associated with new products before they are released for distribution to the field.
    • Assess in the development and improvements of the current Post Market Surveillance processes and work with management to identify problem areas and implement solutions.
    • Coordinates input on data from other functional teams.
    • Supports and performs level II job duties as needed.
    • Performs other duties as assigned

    Qualifications

    Training and Education Bachelor's degree in Scientific Field. Experience
    • 5 year of laboratory experience and troubleshooting molecular tests. Microbiology or clinical lab experience is preferable.
    • Film Array experience preferred
    Knowledge, Skills and Abilities
    • Detail oriented
    • Organizational skills
    • Data analysis
    • Effective writing and communication skills
    • Time management
    • Analytical skills
    • Ability to work independently
    • Ability to follow detailed processes
    • Strong knowledge of the clinical molecular diagnostic field's concepts, practices, procedures, rules and regulations.
    • Knowledge of medical device regulation preferred
    Physical Requirements Physical requirements found in a typical office setting