Category Regulatory Affairs Manager
Há 6 dias
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 OverviewPerrigo 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 RoleStrategic 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.
- 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 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 here
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
-
Regulatory & Public Affairs Specialist
2 semanas atrás
Brasil Kaizen Gaming Tempo inteiro R$90.000 - R$120.000 por anoWe are Kaizen GamingKaizen Gaming, the team powering Betano, is one of the biggest GameTech companies in the world, operating in 19 markets. We always aim to leverage cutting-edge technology, providing the best experience to our millions of customers who trust us for their entertainment.We are a diverse team of more than 2.700 Kaizeners, from 40+...
-
External Affairs Manager
Há 4 dias
Brasil BAT Tempo inteiro R$80.000 - R$120.000 por anoBAT is evolving at pace into a global multi-category business on a mission to decrease the health impact of our industryTo achieve our ambition, we are looking for colleagues who are ready to Be The Change. Come, join us on this journey British American Tobacco Brazil has an exciting opportunity for an External Affairs Manager in Brasilia, BrazilYour key...
-
Clinical Site Manager
4 semanas atrás
Brasil Planet Pharma Tempo inteiroClinical Site Manager – (Ophthalmology & Neurology Focus) Location: Remote-based We’re partnering with a global biopharmaceutical company dedicated to advancing treatments in Ophthalmology, Neurology , and other complex therapeutic areas. To support several ongoing and upcoming studies, we are seeking a Clinical Site Manager to oversee key investigator...
-
Clinical Site Manager
2 semanas atrás
Brasil Planet Pharma Tempo inteiroClinical Site Manager – (Ophthalmology & Neurology Focus) Location: Remote-based We're partnering with a global biopharmaceutical company dedicated to advancing treatments in Ophthalmology, Neurology , and other complex therapeutic areas. To support several ongoing and upcoming studies, we are seeking a Clinical Site Manager to oversee key investigator...
-
Children's Clinical Site Manager
4 semanas atrás
Brasil Planet Pharma Tempo inteiroClinical Site Manager – (Ophthalmology & Neurology Focus) Location: Remote-based We’re partnering with a global biopharmaceutical company dedicated to advancing treatments in Ophthalmology, Neurology , and other complex therapeutic areas. To support several ongoing and upcoming studies, we are seeking a Clinical Site Manager to oversee key investigator...
-
Clinical Site Manager
2 semanas atrás
Índio do Brasil Planet Pharma Tempo inteiroClinical Site Manager – (Ophthalmology & Neurology Focus)Location: Remote-basedWe're partnering with a global biopharmaceutical company dedicated to advancing treatments in Ophthalmology, Neurology, and other complex therapeutic areas. To support several ongoing and upcoming studies, we are seeking a Clinical Site Manager to oversee key investigator sites...
-
Clinical Site Manager
2 semanas atrás
Índio do Brasil Planet Pharma Tempo inteiroClinical Site Manager – (Ophthalmology & Neurology Focus) Location: Remote-based We're partnering with a global biopharmaceutical company dedicated to advancing treatments in Ophthalmology, Neurology, and other complex therapeutic areas. To support several ongoing and upcoming studies, we are seeking a Clinical Site Manager to oversee key investigator...
-
Trust & safety manager [risk & response]
2 semanas atrás
Brasil Kuaishou Technology Tempo inteiroThis role is critical in managing escalations, mitigating risks, and protecting the integrity of our platform and community. Key ResponsibilitiesManage complex escalations from Customer Service and cross-functional teams, including copyright, advertising fraud, hate speech, minor safety, and underage accounts.Handle inquiries and escalations from...
-
Pharmacovigilance specialist consultant
2 semanas atrás
Brasil ClinChoice Tempo inteiroJob Description Job Title: Senior Executive / Specialist - Case Processing Employment Type: Contract Location: Brazil (Remote) About Clin Choice Clin Choice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs,...
-
Account Manager
Há 6 dias
Brasil SHEIN Tempo inteiro R$30.000 - R$60.000 por anoDescriptionJob ResponsibilitiesResponsabilities:● Responsible for improving sales and number of orders for all managed sellers they assist● Responsible for establishing and maintaining a good relationship with fashion sellers, monitoring sales and operation● Help the sellers to select SKUs for various campaigns and promotions● Prepare reports and...