Compliance and Regulatory Expert for Medical Devices

1 day ago


Gothenburg, Västra Götaland, Sweden Cochlear Full time

We are seeking a highly experienced professional to lead our CBAS Regulatory team based in Gothenburg, Sweden. As Director of Regulatory Affairs, you will be responsible for developing and optimizing systems for tracking regulatory submissions and commitments, and leading the team in managing change controls and submission requirements.

About the Company

Cochlear develops world-leading medical devices that help people hear. Our employees tell us that the number one reason they enjoy working for Cochlear is the opportunity to make a difference to people's lives.

As a top 100 medical device company and market-leader in implantable hearing devices, we are committed to helping people hear and be heard. We innovate and bring to market a range of implantable hearing solutions that deliver a lifetime of hearing outcomes.

The ideal candidate will have a strong background in regulatory affairs, excellent communication skills, and the ability to thrive in a fast-paced, dynamic environment.



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