Device Development and Regulatory Expert

3 days ago


Los Angeles, California, United States IntelliPro Group Inc. Full time
Job Description

We are looking for a talented Device Development and Regulatory Expert to join our team at IntelliPro Group Inc. as a Sr. Regulatory Affairs Specialist/Manager. This is an exciting opportunity to work with a dynamic company and contribute to the success of our medical device clients.

In this critical role, you will be responsible for overseeing medical device development and market introduction, ensuring compliance with regulatory standards for Class I, II, and III devices. Your expertise in regulatory affairs will be instrumental in guiding cross-functional teams through the complex process of developing and marketing medical devices.

You will work closely with our clients to provide strategic guidance on regulatory matters, develop and maintain effective quality systems, and prepare and submit regulatory documentation to various authorities. If you have a strong understanding of medical device regulations, excellent analytical and problem-solving skills, and a passion for regulatory affairs, we encourage you to apply.



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