Design a more beautiful world with us
Join the team behind the shimmer in cosmetics, the gleam in concept cars and the science that sparks innovation. At SUSONITY, we don’t just create materials – we bring beauty and performance to life. And we’re just getting started. As a global team of thinkers, makers and innovators, we’re united by a simple belief: that surfaces can do more than look good – they can perform brilliantly. Join us and help build the next generation of beauty, durability and design.
The role
An exciting opportunity is available within our Product Compliance Department. As Senior Regulatory Affairs Expert for Biocides (EU & GB), you will coordinate and execute regulatory activities for our insect repellent business, with a primary focus on the EU Biocidal Products Regulation (BPR, Regulation (EU No 528/2012) and GB BPR. You will also contribute to registration projects across global markets.
Working closely with colleagues in Product Management, Sales and Product Development, you will help ensure that our portfolio meets regulatory requirements and remain fit for market. Following onboarding, you will act as a key regulatory contact for authorities, industry associations and customers. You will become part of a global team responsible for product compliance, sustainability and quality oversight across our portfolio.
Your responsibilities
- Coordinate and execute regulatory activities for the PT19 insect repellent business under the EU and GB BPR at active substance and biocidal product level, including authorisations, renewals, changes and other post-authorisation activities.
- Monitor and assess regulatory developments and their potential impact on our portfolio.
- Contribute to and coordinate regulatory registration projects across international markets.
- Act as a key regulatory contact for competent authorities, industry associations and customers.
- Work closely with global colleagues and cross-functional partners in Product Management, Sales and Product Development.
- Support the global team in ensuring product compliance, sustainability and quality oversight across SUSONITY’s portfolio.
Your profile
- Master’s degree or Ph.D. in natural sciences, preferably with a background in toxicology.
- At least 7 years of professional experience in regulatory affairs under the EU BPR and practical knowledge working under the GB BPR. Professional experience with EU/GB BPR legislation and regulatory requirements, including regulatory procedures at active substance and biocidal product level.
- Experience with human health risk assessments and the interpretation of toxicological data in a regulatory context.
- Practical experience with dossier preparation in IUCLID and dossier submission in R4BP 3.
- Experience with SAP ERP software and document management systems is preferred.
- Strong customer orientation, self-motivation and a genuine interest in networking.
- Very good analytical and process-oriented thinking, combined with a structured, solution-oriented approach.
- Strong interpersonal, verbal and written communication skills, as well as proactive problem-solving and troubleshooting abilities.
- Ability to manage and deliver work in a matrix organisation and to collaborate effectively in a global, cross-functional environment.
- Effective negotiation and presentation skills.
- Fluency in English, both written and spoken, and proficiency in at least one additional major European language.
What we offer
At SUSONITY, you’ll have the opportunity to make a global impact — shaping the commercial foundation of a fast-evolving organization. We offer a culture that values empowerment, collaboration, and innovation, giving you the freedom to lead initiatives that drive real business success.
We support our colleagues in their development and promote an open and inclusive culture. We believe it's our duty to meet our fundamental responsibilities in topics like human rights, labor conditions and anti-corruption practices. We are committed to creating access and opportunities for all to develop and grow at your own pace. People are responsible for the success of our organization, so people play an important role in all we do and how we achieve it.
Apply now and join the bright minds behind brilliant surfaces.
Senior Regulatory Affairs Expert (all genders) Biocides (EU & GB) in Darmstadt Arbeitgeber: Merck
Als Arbeitgeber in Dresden bieten wir Ihnen die Möglichkeit, Teil eines innovativen Teams zu werden, das sich leidenschaftlich für Wissenschaft und Technologie einsetzt. Unsere Unternehmenskultur fördert Vielfalt und Inklusion, während wir Ihnen zahlreiche Möglichkeiten zur beruflichen Weiterentwicklung und persönlichem Wachstum bieten. Mit einem starken Fokus auf Qualität und Sicherheit sowie einem dynamischen Arbeitsumfeld, das Reisen und spannende Herausforderungen umfasst, sind wir der ideale Ort für neugierige Köpfe, die Großes erreichen wollen.