Regulatory Affairs Specialist II – PMA & Class III Devices
Listed on 2026-09-30
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Healthcare
Healthcare Compliance -
Government
K3-Innovations, Inc. is seeking an experienced Regulatory Affairs Associate II in Illinois to support regulatory activities and product approvals in a complex matrixed environment.
You will lead regulatory submissions, review engineering/validation data, and collaborate across functions to ensure on-time approvals for Class III implantable medical devices. The role emphasizes PMA submissions, interactions with FDA, and cross-functional project management in a regulated setting.
The following opportunity is for a Regulatory Affairs Specialist II – PMA & Class III Devices with K3-Innovations, Inc.
Are you ready to take on the Regulatory Affairs Specialist II – PMA & Class III Devices role at K3-Innovations, Inc.?
We would love to welcome a new Regulatory Affairs Specialist II – PMA & Class III Devices to our group in IL, United States.
For the Regulatory Affairs Specialist II – PMA & Class III Devices position at K3-Innovations, Inc., we are reviewing applications now.
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