Category Regulatory Affairs Manager

Perrigouk; Stuttgart; Hybrid; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

An international health and wellness company in Stuttgart is seeking a Regulatory Affairs Manager to lead the regulatory strategy and execution for biocidal products. The ideal candidate will have at least 5 years of experience in regulatory affairs, focusing on compliance excellence and team leadership. Responsibilities include managing the regulatory lifecycle, mentoring staff, and partnering with cross-functional teams to ensure regulatory alignment. This role offers a hybrid working model with competitive benefits.

Leistungen

Competitive compensation

Career development opportunities

Hybrid working flexibility

Qualifikationen

• Minimum 5 years of experience in Regulatory Affairs focused on biocidal products.
• Proven experience with BPR, REACH, and CLP dossier preparation.
• Strong understanding of EU and global regulatory frameworks.

Aufgaben

• Lead regulatory lifecycle management of biocidal products.
• Manage and mentor the Biocides Regulatory Affairs team.
• Collaborate with cross-functional teams for regulatory alignment.

Kenntnisse

Regulatory affairs

Project management

Team management

Stakeholder engagement

Detail-oriented

Analytical

Communication

English fluency

Ausbildung

University degree in Chemistry, Biology, Pharmacy, or related field

Advanced degree preferred

Jobbeschreibung

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London, GB, SW11 7BW Stuttgart, DE, 70173 Sant Cugat del Valles, B, ES, 8174 Chatillon, FR, 92320 Dublin, IE, D02 TY74 Rome, IT, 148 Herrenberg, DE, 71083 Ghent, BE, 9050 Rome, IT, 00147 Chatillon Cedex, FR, 92320

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Join us on our One Perrigo journey as we evolve to win in self-care.

Description Overview

Perrigo is 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 the regulatory lifecycle management of biocidal products, 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 the 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 cross-functional teams including R&D, Quality, Supply Chain, Commercial, and Legal to ensure regulatory alignment and support product development and market access.
• Actively contribute to 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 product authorizations under the Biocidal Products Regulation (EU BPR).
• Maintain up-to-date knowledge of EU and international regulatory requirements for biocidal products, including emerging trends and 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.

Hybrid Working Approach
We love our offices and the setting they provide for in‑person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out morehere

Applicants please note:To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.

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