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Regulatory Affairs Specialist
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Full-time
- Job Title: Regulatory Affairs Specialist
- Location: 63103, St Louis, Missouri, United States
- Duration: 24 Months
- 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.
- Independently assemble and maintain technical files and other regulatory documentation to ensure timely registrations and renewals.
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