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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 weeks 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 weeks ago seen See more...
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Medical Device Regulatory Affairs Consultant (medlance.co)
Medlance
Remote
$30 - $300 an hour
Guide Medical Device companies through the regulatory process. Prepare and submit documentation for FDA and other regulatory bodies. Ensure compliance with all regulatory requirements. Collaborate with cross-functional teams to ad...
a month ago seen See more...
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