Perform toxicological risk assessments for medical devices and combination products
Coordinate with internal laboratories to ensure high-quality data for regulatory submissions
Guide regulatory submissions for FDA and EU compliance and serve as a subject matter expert
Required Qualifications:
Master's degree in Toxicology or a related field
Board Certified Toxicologist or actively pursuing certification
4-6 years of relevant experience in toxicology, with a focus on medical devices
Advanced knowledge of regulatory environments and toxicology standards
Experience with chemical characterization and extractables/leachables studies
Average salary estimate
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$0K
$0K
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