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Group Regulatory Affairs Specialist Class II needed in Großpostwitz, Germany. Ensure market access for medical devices by mastering US and Canada regulations, ISO 13485, and 510k submissions. Leverage 3+ years of RA experience to guide cross-functional teams and navigate SAMD requirements. Join O...
Location
Germany , Grosspostwitz
Salary
Not provided
Ontex Peninsular
Expiration Date
Until further notice
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