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General Quality & Regulatory Affairs Expert 2
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Full-time
- BEPC has an open position for a General Quality & Regulatory Affairs Expert 2 in St. Louis MO!
- With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products, and changes to products or sale of products ensuring continual compliance to all applicable regulations and ensuring that site regulatory strategy aligns with overall corporate regulatory strategy, goals, and objectives.
- Bachelor's or Masters degree in Pharmacy, Chemistry, Biology, Engineering, or other Life Science discipline
- 2+ years of professional experience in Regulatory Affairs (IVD)
- Experience with in-vitro diagnostics
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