Regulatory Affairs Specialist

Job Summary

Supporting Perrigo's non-medicinal portfolio, the full-time Regulatory Affairs Specialist will manage lifecycle activities, including regulatory documentation and compliance for products such as cosmetics and medical devices, while working in a hybrid environment.

Key responsibilities

• Manage lifecycle regulatory activities, including preparation and maintenance of regulatory documentation and product information files
• Independently assess and execute complex post-market lifecycle changes and regulatory filings across multiple products and markets
• Lead cross-functional collaboration to ensure compliance with regulatory requirements and improve lifecycle processes

Required qualifications

• 3-5 years of experience in Regulatory Affairs with a relevant scientific or technical degree preferred
• Practical experience in lifecycle submissions and dossier maintenance
• Ability to represent Regulatory in project teams and lead defined workstreams