 RemoteOtter
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The Senior Regulatory Affairs Manager - Oncology will lead regulatory support for IVD/CDx products, managing FDA submissions and ensuring compliance throughout the product lifecycle.
M.A.T.M
MX00 Agilent Technologies Mexico
Join Agilent as an International Regulatory Affairs Specialist to coordinate regulatory submissions for IVD products in the EMEA region.
Seeking a Sr. Regulatory Affairs Manager to ensure compliance with global regulatory requirements for diagnostics and IVD products.
IMMY
IMMY
The Director of Regulatory Affairs and Design Assurance will lead regulatory strategy and ensure compliance for medical devices and IVDs.
Join NeoGenomics as a Senior Project Manager to lead product development projects in a dynamic remote environment.
Xcenda
Xcenda
The Senior Manager for Medical Writing will prepare technical documentation for IVD medical devices in compliance with EU regulations.
Join RQM+, the largest consulting firm in medical device and diagnostics, as a Regulatory and Quality Consultant.
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