Senior Specialist Regulatory Affair jobs in Kansas
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REGULATORY AFFAIRS SPECIALIST III
Under direct supervision of the RA Project Manager, or Department Manager, assists in preparing moderately complex submissions to gain approvals for clinical research, export, and commercial distribution, such as: IDE, IDES, IDE...
| Company | Boston Scientific |
|---|---|
| Address | Maple Grove, MN |
| Category | Information Technology |
| Date Posted | 2 weeks ago See detail |
Regulatory Affairs Specialist III
Boston Scientific
Maple Grove, MN
Under direct supervision of the RA Project Manager, or Department Manager, assists in preparing moderately complex submissions to gain approvals for clinical research, export, and commercial distribution, such as: IDE, IDES, IDE...
2 weeks ago seen See more...
- View all - jobs in Maple Grove, MN
Sr. Specialist, Regulatory Affairs CMC
Biospace
United States
Prepare content of CMC documentation for large and small molecule product submissions to regulatory agencies (FDA/EMA), ensuring accuracy, completeness, and consistency with strategy. Review and edit final documents for regulatory...
a month ago seen See more...
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Senior Manager, Regulatory Affairs Vendor Governance
Biospace
California, United States
Own initiatives and day to day responsibilities in support of vendor oversight within RA. Negotiation and problem solving between Gilead RA leads and Vendor resources. Able to gather information or assign tasks or activities for o...
a month ago seen See more...
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