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.
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 ...
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 ...
Jul 31 -
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