Job Details

The primary function will be to manage and organize all quality documentation that is required by Globus Medical, Inc. and other regulatory agencies. This will include issuing, maintaining, controlling, and auditing documentation that is required for quality and cGMP compliance. The primary responsibilities of the position include the following:Essential Functions:Issues Quality System documents and coordinate the training process. Issues device master record documents (manufacturing process specifications, inspection plans, routers, etc.) and other technical documents during the development, release, and maintenance phases of product realization. Processes Document Change Orders (DC - Os) to implement all controlled documentation and maintain the distribution of controlled copy documents. Organizes and communicates status of work to management and other personnel as required and keeps them informed of objectives and progress. Ensures documentation is complete, properly formatted and m...Control Specialist, Business Systems, Specialist, Control, Product Development, Healthcare, Training