At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it’s providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world’s most talented people are choosing to work at DuPont. Why Join Us | DuPont Careers

Are you passionate about advancing patient safety and sustainable innovation in healthcare packaging?

DuPont is seeking a Regulatory Science & Standards Manager f/m to lead regulatory scientific affairs and standardization activities across the EMEA region and globally. In this role, you will :

Join DuPont's global Tyvek® sustainability and regulatory team, concentrating on the healthcare packaging sectorChampion state-of-the-art regulatory science, bridging innovation and compliance to deliver safe, effective, and sustainable solutions for the healthcare industryActively contribute to the development and implementation of standardization and stakeholder collaboration strategies, executing initiatives across the EMEA region and globally to support business objectives with efficiency and expertise.

Key ResponsibilitiesAdvocate for patient safety and sustainable innovation based on sound regulatory science advancing the state-of-the-art.Interpret regulatory requirements for DuPont, customers, packaging manufacturers, medical device and pharmaceutical companies, and healthcare facilities.Monitor, analyze and anticipate regulatory developments, leveraging real-world evidence.Remain informed about developments in healthcare packaging and regulatory science literature; publish research in relevant areas to contribute to advancements in the field.Shape and execute global regulatory and standardization strategies.Collaborate with regulators, industry associations, targeted standard development organizations and academic partners to support the development of standards and policy.Support development of product literature, product data and compliance strategies.Support product lifecycle oversight, bringing in regulatory science, including into risk management, product development, change control and post-market surveillance.Deliver presentations at customer events and external conferences.

Qualifications

- Master’s degree or higher in a relevant scientific or engineering discipline.

- Expertise in regulatory science for medical devices, including risk management and chemical/biological aspects of materials.

- The following qualifications and experience, if available, are considered important assets:

Knowledge in clinical aspects, studies and investigations of sterile medical devices with a track record of reviewing current scientific literatureIn-depth understanding of medical device standards and testingExperience achieving market access with conformity assessment bodiesExperience in pharmaceutical applications or combination productsExperience in authoring peer-reviewed scientific papers or articlesExperience integrating sustainability principles into regulatory science and healthcare packaging (e.g., life cycle assessment, circularity, decarbonization).

- Experience developing ISO or CEN standards (or willingness to acquire).

- Experience working with industry associations is a strong asset.

- Strong networking, collaboration, and negotiation skills.

- Excellent writing, communication and presentation skills.

- Innovative and entrepreneurial mindset with strategic thinking skills.

- Fluency in English required; additional languages (German, French) are a strong plus.

- Multi-cultural experience and willingness to travel globally.

What We OfferCompetitive salaries and comprehensive benefitsAnnual variable pay program rewarding team and individual performanceOngoing learning and development opportunitiesCareer experiences across different businesses and functionsThe chance to work on global teams with colleagues worldwide

Ready to make an impact in sustainable healthcare packaging? Apply today and join DuPont’s global team!

#LI-CD1

Join our Talent Community to stay connected with us!

DuPont is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information.

DuPont offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.