Global Medical Device Regulatory Lifecycle Specialist in London

Global Medical Device Regulatory Lifecycle Specialist in London

London 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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Global Medical Device Regulatory Lifecycle Specialist in London employer: Perrigo Company

Perrigo Company plc is an exceptional employer located in the vibrant city of London, offering a dynamic work culture that fosters collaboration and innovation. Employees benefit from comprehensive growth opportunities within a multinational finance environment, where they can enhance their skills in core accounting processes and financial reporting while contributing to meaningful projects that impact the North Europe Cluster.

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Contact Details:

Perrigo Company Recruitment Team