REQUIRES 5 YEARS OF EXPERIENCE IN REGULATORY AFFAIRS. REQUIRES 5 YEARS OF EXPERIENCE IN ORTHOPEDIC OR MEDICAL DEVICE INDUSTRY AND WITH EU, EMEA, APAC, LATAM, OR US REGULATIONS PERTINENT TO MEDICAL DEVICES, BIOLOGICS, DRUGS AND COMBINATION PRODUCTS. REQUIRES 2 YEARS OF EXPERIENCE COORDINATING WITH OTHER BUSINESS UNIT REGULATORY AFFAIRS TEAMS THAT HAVE ESTABLISHED GTS CONNECTIONS; WITH REGULATORY AFFAIRS OBJECTIVE EVIDENCE NEEDED TO SUPPORT DISTRIBUTION CONTROLS; 2 YEARS OF EXPERIENCE IN LEADING AND MANAGING REGULATORY AFFAIRS TEAMS INVOLVED IN MAINTAINING GLOBAL REGISTRATIONS; 2 YEARS OF EXPERIENCE WORKING EXPERIENCE WITH SYSTEMS AND SAP ERP. REQUIRES 1 YEAR OF EXPERIENCE PROVIDING REGULATORY AFFAIRS TRAINING TO ENTRY LEVEL REGULATORY AFFAIRS ASSOCIATES, INTERNS, ANALYSTS, OR SPECIALISTS ON REGULATORY AFFAIRS SYSTEMS, REGULATIONS AND PROCESSES.
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