Principal Regulatory Affairs Specialist jobs in Minnesota
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PRINCIPAL REGULATORY AFFAIRS SPECIALIST (MEDLANCE.CO)
Lead regulatory strategy development for medical device projects. Manage submissions to regulatory bodies. Advise on regulatory requirements and changes. Collaborate with cross-functional teams for regulatory compliance. Extensive...
| Company | Medlance |
|---|---|
| Address | Remote |
| Category | Education/Training |
| Salary | $30 - $300 an hour |
| Job type | Contract |
| Date Posted | 2 months ago See detail |
Principal Regulatory Affairs Specialist (medlance.co)
Medlance
Remote
$30 - $300 an hour
Lead regulatory strategy development for medical device projects. Manage submissions to regulatory bodies. Advise on regulatory requirements and changes. Collaborate with cross-functional teams for regulatory compliance. Extensive...
2 months ago seen See more...
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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...
a week ago seen See more...
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Regulatory Affairs Specialist
Redbock- An Nes Fircroft Company
Remote
$70.9K - $89.8K a year
Prepare and maintain international submission dossiers. Prepare electronic pre-market and post-market regulatory submissions. Compile Technical Documentations for IVD medical devices. Monitor progress on project deliverables and p...
2 months ago seen See more...
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Regulatory Affairs Specialist
Brs
Remote
$62.1K - $78.7K a year
Contractor shall have at least 5 years experience applying FDA research regulatory requirements within a research Regulatory Affairs program office. Work in preparing ones own research proposals and ones own submissions to an IR...
2 months ago seen See more...
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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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