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Job Duties Support the VP of Global Regulatory Affairs Operations in strategic planning and execution. The Operations Manager will work directly with the VP of Global Regulatory Affairs Operations to ensure the smooth and efficient delivery of QARA programs and goals.
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8+ years relevant experience in quality control, quality assurance, and regulatory affairs at a Class I or Class II medical device manufacturer. Coordinate and organize test data and clinical or scientific reviews in support of regulatory submissions.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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May oversee and direct the work of other Regulatory Affairs professionals. Serves as a regulatory liaison for new product development and make regulatory assessments of proposed changes to existing products for impact to regulatory documentation.
$116,030 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Manage communications with the US FDA, Health Canada, notified bodies and other regulatory agencies/authorities. Conduct regulatory research. B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry.
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Support the VP of Global Regulatory Affairs Operations in strategic planning and execution. Experience in Regulatory Affairs within the medical device industry (minimum 5 years), with specific management experience, ideally in a matrix organization.
$156,345 a yearFull-timeExpandApply NowActive JobUpdated 24 days ago
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