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manufacturing 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: Maintenance of Domestic and International listings, registrations and technical documentation Preparation of internal regulatory file documentation Preparation of documents, i.e. 510(k)s, STEDs for submission to various ...

  2. Quality Engineer I

    Location: Jacksonville, FL Validation Lead II I. Write a brief summary statement of the basic purpose(s) of this position, i.e., why the position exists and its purpose in the organization. Manage the development & implementation of software validation policies and procedures. Manage/conduct software validation projects in support of existing computerized systems in the Jacksonville campus. Project responsibilities will be focused on medium to large validation projects. This position may also ...