Regulatory Affairs Manager – Category Regulatory Affairs Manager – Perrigo Company plc
Perrigo is a global leader in health and wellness solutions that improves lives through trusted, high-quality products. We are committed to inclusive culture, continuous learning and delivering excellent value to our consumers and stakeholders.
Description Overview
We are seeking a dynamic and experienced Regulatory Affairs Manager to lead regulatory strategy and execution for our biocidal product portfolio across multiple territories. This role offers a unique opportunity to shape regulatory pathways, drive compliance excellence, and lead a high-performing team within a fast‑paced, innovation‑driven environment.
Scope of the Role
Strategic Regulatory Leadership
* Lead biocidal product lifecycle management, including licensing, renewals, variations, and post‑marketing activities.
* Develop and implement regulatory strategies aligned with business objectives and evolving regulatory frameworks (e.g., BPR, REACH, CLP).
* Serve as subject‑matter expert on biocides, providing strategic guidance to internal stakeholders and senior leadership.
Team Management & Development
* Manage and mentor the Biocides Regulatory Affairs team, fostering a culture of accountability, collaboration, and continuous improvement.
* Set clear objectives, monitor performance, and support professional development within the team.
Cross‑Functional Collaboration
* Partner closely with R&D, Quality, Supply Chain, Commercial, and Legal to ensure regulatory alignment and support product development and market access.
* Actively contribute regulatory input in innovation projects, product launches, and strategic business initiatives.
Technical Excellence
* Prepare, review, and submit high‑quality regulatory dossiers for active substances and products under the Biocidal Products Regulation (EU BPR).
* Maintain up‑to‑date knowledge of EU and international biocide regulatory requirements and emerging legislative changes.
* Ensure regulatory compliance across all relevant markets and proactively manage regulatory risks.
Experience Required
* University degree in Chemistry, Biology, Pharmacy, or related scientific discipline; advanced degree preferred.
* Minimum 5 years of experience in Regulatory Affairs with a strong focus on biocidal products and chemical regulations.
* Proven experience in preparing and submitting dossiers under BPR, REACH, and CLP.
* Demonstrated leadership experience, including team management and stakeholder engagement.
* Strong understanding of regulatory frameworks across EU and global markets.
* Excellent project management skills with the ability to manage multiple priorities and deadlines.
* Fluent in English; additional European languages are a plus.
* Strategic thinker with a hands‑on approach and a passion for regulatory excellence.
* Strong interpersonal and influencing skills with the ability to build trust and drive alignment across diverse teams.
* Detail‑oriented, analytical, and solution‑focused.
* Resilient and adaptable in a dynamic regulatory and business environment.
* Committed to continuous learning and professional growth.
Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally. Find out more about Total Rewards at Perrigo.
Hybrid Working Approach
We support flexibility with the ability to work two days a week from home in many roles while encouraging in‑office collaboration and celebration.
We are proud to be included in the Forbes list of "America's Best Employers by State 2024".
Equal Opportunity Employer Statement: We are an equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran or other characteristics protected by law. #weareperrigo
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