Global Medical Device Regulatory Lifecycle Specialist

Global Medical Device Regulatory Lifecycle Specialist

Full-Time No working from home possible
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Perrigo Company plc is seeking an Associate Professional, Regulatory Affairs to support lifecycle regulatory activities for our medical device portfolio across markets. You will help manage technical documentation, regulatory records, and labeling updates under guidance within a dynamic global environment.

The role offers exposure to diverse regulatory landscapes and a platform to contribute to compliant product lifecycle management.

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Contact Details:

Perrigo Company Recruitment Team