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Regulatory Affairs Specialist Our client is currently seeking a Regulatory Affairs Specialist. Education: BA/BS in Science, Engineering, Legal, or Regulatory, Advanced degree and/or RAC(s) preferred. Experience: 3+ years of experience within medical device or other regulated industry. Knowledge of FDA Quality System Regulations (21 CFR), EU Medical Device Directives (MDD)and applicable guidance documents. Familiarity with EU Medical Device Regulation (MDR) and additional international regulations preferred. 510(k), IDE,. After registering you may be able to apply for this job directly (if still active) on (The Judge Group)'s site. Future job matches may be sent from Geebo approved job partners.
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