Senior Regulatory Affairs Specialist, Global Medical Devices

Jena Valve Technology, Inc. seeks a Senior Specialist, Regulatory Affairs to manage global regulatory submissions, collaborate with cross-functional teams, and ensure compliance for medical devices in the Irvine, CA office.

This role supports post-market surveillance, adverse event reporting, and regulatory strategy. The candidate will interact with regulatory authorities, prepare submissions, and help translate complex regulations into actionable plans while maintaining quality system alignment

Step into the Senior Regulatory Affairs Specialist, Global Medical Devices role at Jena Valve Technology, Inc. in Irvine, CA, United States and grow with us.

This role, Senior Regulatory Affairs Specialist, Global Medical Devices at Jena Valve Technology, Inc., could be your next opportunity.

Are you ready to take on the Senior Regulatory Affairs Specialist, Global Medical Devices role at Jena Valve Technology, Inc.?

We would love to welcome a new Senior Regulatory Affairs Specialist, Global Medical Devices to our team in Irvine, CA, United States.