• Regulatory Affairs Specialist - 1349

    Job Locations CA-ON-Mississauga
    Job ID
    2018-1414
    Category
    Quality, Regulatory Affairs, and Service
    Type
    Full-Time/Regular
  • Overview

     

    ZOLL Medical is a growing, innovation-driven company on the forefront of delivering medical devices to save lives, and software solutions to improve efficiency. With customers in more than 140 countries, we continue to expand our reach, as well as our product offerings. Hospitals, emergency medical services (EMS), and others trust us to provide high-quality products and exceptional customer service. ZOLL products are used every day across the globe to save the lives of people who suffer sudden cardiac arrest. From Real CPR Help® technology—an industry first—to the world’s only wearable defibrillator, our capabilities and features set us apart. But none of this would be possible without the motivation and dedication of ZOLL employees, and we’re invested in their success.

     

    We offer competitive salaries and a comprehensive benefits package. Join our team. It’s a great time to be a part of ZOLL!

     

    Job Summary:

     

    Responsible for the implementation and administration of organization activities to support and ensure regulatory compliance.

     

     

    Responsibilities

     

    • Understands and has working knowledge of FDA medical device regulations, European Medical Device Directives, and/or other global regulations.
    • Participates in product core teams as required to ensure that the product is in compliance with all internal and external regulatory requirements. Develops, documents and implements a regulatory strategy plan around product development goals.
    • Prepares U.S. FDA submissions (e.g., 510(k), IDE, PMA) as required and per applicable SOPs.
    • Initiates and updates technical files/dossiers/registrations as required and per applicable SOPs.
    • Reviews and approves change orders for compliance with FDA, European and/or global regulations and standards.
    • Implement submission templates
    • Monitors and maintains regulatory files in good order.
    • Maintains current knowledge of device regulations, guidance and standards applicable to device product submissions. Analyzes the information and provides updates.
    • Participates in departmental improvement activities. Makes recommendations for process improvements to improve efficiency and accuracy of device submissions and other procedures.
    • Assist with device recall activities
    • Participate as an auditor in internal audit activities
    • Review, disposition and approve Engineering Change Requests
    • Other duties as assigned
    • Some travel is required ~10%

     

    Qualifications

     

    • Demonstrated working knowledge of scientific principles
    • A self-starter with the ability to work independently with minimal supervision and as part of a small team
    • Very detail-oriented, well organized, and driven to meet deadlines and program goals
    • Strong verbal and written communication skills
    • Good computer skills with knowledge of Microsoft Office.
    • Knowledge of FDA, European, Canadian and Japanese Regulatory Requirements
    • Ability to multitask and prioritize 

    Required/ Preferred Education and Experience:

    • Four-year college degree with 3-5 years related experience or a Master's Degree in a Regulatory Affairs or related discipline.

     

    Other Duties:

     

    Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities will be reviewed periodically as duties and responsibilities change with business necessity. Essential and marginal job functions are subject to modification. #LI-NM1

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