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Our client is in the process of transitioning their manufacturing facility to a new location. During the transition the client is taking the opportunity to update some of their older technical files to make sure they are in compliance.Medical Device Project Manager
This consultant will be responsible for various tasks that involve getting the site up and running. They will be handling all necessary updates to regulatory documents from a regulatory compliance standpoint. This consultant will have ideally worked on a manufacturing site transfer before in orderhit the ground running. This person will not be responsible for any Regulatory Submissions.Medical Device Risk Management SME Required Skills: Supplier Quality Engineer
5+ Years Experience Regulatory Compliance for Medical Device Manufacturing
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