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document control in Jacksonville

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    1. Global Regulatory Affairs Specialist

      The Global Regulatory Specialist will provide support and maintain compliance for existing registrations world-wide ensuring that medical device products are cleared for sale and remain in compliance with applicable standards and country regulations.   Responsibilities: ...

    2. Associate Quality Engineer

      The Associate Quality Engineer supports new methods or procedures to reduce risk related to equipment, materials, processes, products and or technical methods. The Associate Quality Engineer will utilize Quality Engineering tools and practices for the effective and efficient ...