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Actalent Regulatory Affairs Associate III in Round Lake, Illinois

Description:

Will author regulatory submissions for the US and EU Will develop regulatory strategy for medical device products Will work with cross functional teams Will communicate with external regulators and notified bodies to respond to inquiries

Skills:

Regulatory Affairs, Medical Device, Regulatory Submissions, FDA, GMP, GDP, Notified Bodies, 510k

Top Skills Details:

Regulatory Affairs,Medical Device,Regulatory Submissions

Additional Skills & Qualifications:

BS Degree 5+ years of experience authoring regulatory submissions for medical device products Experience with US and EU regulations

Experience Level:

Expert Level

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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