Category Regulatory Affairs Manager

vor 2 Wochen


Stuttgart, Deutschland Perrigo Vollzeit

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. BenefitsWe 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 at Perrigo. Hybrid Working ApproachWe 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 more 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



  • Stuttgart, Baden-Württemberg, Deutschland Real Vollzeit 60.000 € - 80.000 € pro Jahr

    Regulatory Affairs Specialist (m/w/d)Aktuell suche ich für unseren Kunden, ein mittelständisches Medizintechnikunternehmen in Baden-Württemberg einen Regulatory Affairs Spezialisten (m/w/d) in unbefristeter Festanstellung.Ihre Aufgaben:Unterstützung bei der internationalen Zulassung von MedizinproduktenErstellung und Pflege von technischen...

  • Regulatory Affairs

    vor 2 Wochen


    Stuttgart, Deutschland YiDa Business Consulting & Translation Services Vollzeit

    About our client Our client, for whom we are looking for a  Regulatory Affairs & Product Compliance Manager (full-time job) is the subsidiary of a Fortune Global 500 company in the field of Home Appliance.  Qualifications and knowledge: Minimum bachelor’s degree in engineering, Regulatory Affairs, or a related field (Master’s or higher preferred). At...


  • Stuttgart, Deutschland Steffen Glaser Personalberatung Vollzeit

    _**Regulatory Affairs Professional EMEA - Medical Devices (m/w/d)**_ **Job-ID**: 776 **Standort**: Baden-Württemberg (Office oder hybrides Arbeiten möglich) Unser Auftraggeber ist ein schnell wachsender Hersteller von innovativen Klasse-3-Medizinprodukten und Teil einer erfolgreichen, international aufgestellten Unternehmensgruppe der Medical Device...


  • Stuttgart, Baden-Württemberg, Deutschland pates GmbH Vollzeit 67.500 € - 75.000 € pro Jahr

    6545MedizintechnikFestanstellung Vor OrtBaden-WürttembergKurzbeschreibung:Internationale Zulassungen steuernRegulatorische Verantwortung übernehmenModerne Arbeitswelt erlebenEin international tätiges, etabliertes Unternehmen aus dem Dentalbereich sucht im Zuge des weiteren Wachstums eine fachlich versierte Verstärkung für den Bereich Regulatory Affairs....


  • Stuttgart, Deutschland KLS Martin Group Vollzeit

    Head of Regulatory Affairs International Registration (m/w/d) Die KLS Martin Group ist ein global agierendes, mittelständisches Familienunternehmen der Medizintechnik. Seit 1896 und mit rund 1.800 Mitarbeitern weltweit widmen wir uns der Chirurgie und entwickeln umfassende medizintechnische Problemlösungen. Werden auch Sie ein Teil davon und tragen Sie so...


  • Stuttgart, Deutschland bioMérieux sa Vollzeit

    A family-owned company, bioMérieux has grown to become **a world leader in the field of in vitro diagnostics**. For almost 60 years and across the world, we have imagined and developed **innovative diagnostics solutions** to **improve public health**. Today, our teams are spread across 44 countries and serve 160 countries with the support of a large...


  • Stuttgart, Deutschland ecm partners Vollzeit

    ecm partnersUnser Klient gehört zu den Marktführern und Innovationstreibern auf dem Gebiet der intelligenten Systemkomponenten für die Fabrikautomation und ist technologischer Partner für verschiedene Segmente des Maschinen- und Anlagenbaus und der Intralogistik. Das Unternehmen verfügt über zahlreiche Niederlassungen weltweit und erwirtschaftet einen...


  • Stuttgart, Deutschland Wörwag Pharma Vollzeit

    Wörwag Pharma - ein mittelständisches, international tätiges Pharmaunternehmen in Familienbesitz mit Hauptsitz in Böblingen bei Stuttgart, das sehr früh die Bedeutung von Biofaktoren erkannt und wissenschaftlich belegt hat. Seit über 50 Jahren sagen wir den Zivilisationskrankheiten unserer Zeit den Kampf an - vorbeugend, begleitend, heilend. Bei uns...


  • Stuttgart, Baden-Württemberg, Deutschland Cogs Vollzeit 80.000 € - 120.000 € pro Jahr

    About the Role: Our client in the Chemical Industry is seeking a highly skilled and motivated Senior Global Category Manager specializing in Chemicals to join their procurement team. In this strategic role, you will be responsible for managing the global chemicals category, driving cost efficiencies, and ensuring the supply of high-quality materials for our...


  • Stuttgart, Deutschland Erbe Elektromedizin GmbH Vollzeit

    **Über uns**: Als inhabergeführtes Familienunternehmen entwickeln, produzieren und vertreiben wir weltweit chirurgische Spitzentechnologie. Durch unsere zukunftsorientierte Unternehmensführung treiben wir den medizinischen Fortschritt voran und leben Werte wie Vertrauen, Respekt und Offenheit. Das ist die Basis unseres Erfolgs. Für** unseren Standort in...