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Manager, Regulatory Affairs
  **The ideal candidate must reside in or be willing to relocate with company financial assistance to Marietta/Atlanta, Georgia. This position will be eligible for a hybrid work schedule following 90 days of employment.**   Essential Responsibilities Creates, revises, and implements quality standards as well as procedures [i.e., Standard Operating Procedures (SOPs), etc.] for Erbe USA's Quality Management Systems as an initial importer and distributor of medical devices in the United States. This includes updating all Systems to new/revised requirements by FDA. Back up to the Sr. Director of Quality & Regulatory Affairs as the quality representative for Erbe USA. Informs Erbe USA executives and oth


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