Zimmer Biomet Holdings Inc logo

Product Surveillance Coordinator

Zimmer Biomet Holdings Inc
  • IN
    27 days ago

    Job Description

    At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

    As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

    What You Can Expect

    This position is responsible for receiving, documenting, and triaging complaints. This role ensures that all complaints are captured accurately, assessed promptly, and routed to the appropriate teams for investigation within a defined process. Decision making and assessments are limited to those clearly defined within the applicable corporate and site procedures.

    How You'll Create Impact

    Principal Duties and Responsibilities:

    • Receive and log complaints via phone, email, web portals, and other channels.
    • Collect and document all relevant details to ensure accurate and complete complaint records in a timely manner as defined in procedures.
    • Perform initial triage to categorize complaint type, severity, and urgency.
    • Adheres to all corporate and site-specific procedures.
    • Identifies and investigates solutions to procedure and process related issues.
    • Monitors appropriate metrics to measure key performance indicators of the unit.

    This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.

    What Makes You Stand Out

    Expected Areas of Competence (i.e., knowledge, skills and abilities):

    • Good organization and time management skills
    • Detail-oriented
    • Knowledge of EtQ, JD Edwards, Internet, Microsoft Office applications and the ability to learn other software quickly as required.
    • Ability to consistently meet high standards of input accuracy, produce quality documents, compile data, and perform simple analyses with accuracy.
    • Good decision making skills and proven ability in balancing priorities among the many ongoing tasks, and being responsive to critical situations, as this position has a high volume of work, regulatory mandated time limits, and often changing priorities.
    • Proven ability to work in a team setting. Ability to work closely with others.

    Your Background

    Education/Experience Requirements:

    • High school diploma or equivalent required
    • 2+ years' of experience in technical writing, regulatory compliance, report generation, or an equivalent combination of education and experience, preferred.

    Travel Expectations

    5%

    EOE/M/F/Vet/Disability

    Numbers & Facts

    LocationIN
    IndustryMedical Devices and Supplies
    Year Founded1927
    Websitehttp://www.zimmer.com/

    About Company

    Do you find pride and purpose in helping millions of people around the world renew their lives? If so, career opportunities at Zimmer facilities worldwide will be an excellent fit for you. We're looking for remarkable people who can be catalysts for change, collaborate globally and push the boundaries of innovation so that we can continue to make the world a more mobile place. We've found that when you're working to improve others' lives, you start to feel incredibly proud and excited about what you do. Join us and find your fit in a company with passion.

    Skills

    • High School Diplomaunmatched
    • Internet Portalunmatched
    • Metricsunmatched
    • Organizational Skillsunmatched
    • Patient Assessmentunmatched
    • Performance Metricsunmatched
    • Procedure Developmentunmatched
    • Regulatory Complianceunmatched
    • Regulatory Reportsunmatched
    • Surveillanceunmatched
    • Team Playerunmatched
    • Technical Leadershipunmatched
    • Technical Writingunmatched
    • Time Managementunmatched

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