[Hiring] Senior Regulatory Affairs Expert @SUSONITY Commercial

Role Description

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 remains 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.

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.

Qualifications

• 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.

Benefits

• Opportunity to make a global impact — shaping the commercial foundation of a fast-evolving organization.
• A culture that values empowerment, collaboration, and innovation.
• Freedom to lead initiatives that drive real business success.
• Support in development and promotion of an open and inclusive culture.
• Commitment to meeting fundamental responsibilities in topics like human rights, labor conditions and anti-corruption practices.
• Access and opportunities for all to develop and grow at your own pace.