About the role

Perrigo seeks a Regulatory Affairs Professional within Non-Medicinal Lifecycle Management to support cosmetics, VMS, general products and medical devices across the lifecycle. You will manage lifecycle activities, prepare and maintain regulatory documentation, and coordinate filings across markets, partnering with Quality, Safety, and R&D to ensure timely, compliant submissions and supply continuity. Hybrid work options are available, with partial remote days, and you will contribute to process

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JOB OVERVIEW

Experience level

Senior

Location

Martin, MI

Occupation

Regulatory Affairs Specialists

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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