Regulatory Affairs Manager

Regulatory Affairs Manager - Novel Technology Location: Home Working / Teletravail - France Introduction Our client is an innovative and fast-growing company operating at the intersection of science, sustainability, and modern agriculture. Founded on cutting-edge research, the business is redefining how crop protection challenges are addressed by developing alternative, environmentally responsible solutions that move beyond conventional chemistry. With strong financial backing, a growing international footprint, and ambitious expansion plans, the company offers a collaborative and science-driven working environment where regulatory expertise plays a central strategic role.This is an excellent opportunity for an experienced Regulatory Affairs professional to take ownership of complex EU regulatory activities and contribute directly to the long-term success and credibility of a highly differentiated technology platform. Why our Client?The company operates in a highly specialised niche where regulatory strategy is not a support function but a core value driver. Because its solutions are based on innovative modes of action and novel regulatory pathways, the Regulatory Affairs Manager will be deeply involved in shaping submission strategies, interacting with authorities, and guiding projects from early development through to approval. This provides the benefit of genuine ownership, intellectual challenge, and long-term visibility within the organisation.Growth is a defining feature of the business. With multiple products progressing through development and regulatory phases simultaneously, the role offers exposure to a broad and evolving portfolio across chemical and biological solutions. As the company scales, regulatory expertise will be critical to enabling market access, making this position well-placed for professional progression and increasing responsibility as the organisation expands. Within the next 1 to 2 years, this role will take on a global dimension where you will be responsible for Regulatory Activities across LATAM and other major markets.The working culture combines scientific rigour with pragmatism and agility. Small enough to remain flexible and collaborative, yet sufficiently established to offer stability and resources, the company encourages close interaction between regulatory, R&D, development, and commercial teams. This creates an environment where regulatory decisions are respected, well-informed, and clearly linked to business outcomes.Key ResponsibilitiesManage and coordinate EU regulatory dossiers for active substances and formulations under Regulation 1107/2009Lead regulatory strategy for new and renewal submissions at EU and national levelsCoordinate data gap analysis, dossier planning, and submission timelinesMonitor and manage GLP studies across toxicology, ecotoxicology, residues, environmental fate, physico-chemistry, and analytical methodsAct as a key regulatory interface with authorities, including Rapporteur Member States and EFSASupport internal stakeholders across development, marketing, and commercial teams with regulatory guidanceManage and contribute to task forces and external consultant/CRO interactionsContribute to regulatory activities related to fertilisers and biostimulants under Regulation 2019/1009 where applicableKey RequirementsSignificant experience in Regulatory Affairs within the agrochemical or biosolutions sectorProven track record managing EU active substance and/or product registration dossiersStrong working knowledge of Regulation 1107/2009 and EU regulatory processesExperience coordinating GLP studies across multiple scientific disciplinesAbility to manage complex projects, timelines, and multiple stakeholdersExperience interacting with EU regulatory authorities and assessment bodiesStrong scientific background in environmental sciences, biology, chemistry, or related fieldsFluent English; additional European languages advantageousAdditional InformationThis role offers a high level of autonomy, exposure to innovative technologies, and the opportunity to influence regulatory strategy within a growing organisation. The company supports flexible working practices and values collaboration, scientific integrity, and long-term thinking. The position is well suited to someone seeking both stability and the opportunity to help shape the future direction of a business operating in a rapidly evolving regulatory landscape.If you are ready to take the next step in your career with a Biotech with high potential, please apply on here or send your CV to b(.)thomson(@)nonstopconsulting(.)com with ref: BT.772515.1 / Please Note: Due to the time of year, I will be out of the office until the 5th of January 2026 and will endeavour to respond to application as early as possible.Affairs recruiter in Europe with a distinguished track record of placing candidates with top companies and consultancies in the Agrochemicals and associated sectors. Even if this particular opportunity isn't the perfect fit, we may have other exciting roles that align with your expertise - so don't hesitate to get in touch Key Words: Regulatory Affairs| Registrations | Toxicologist | Ecotoxicology | Residues |Phsychem |Environmental Fate | 1107/2009 | Agrochemical | Crop Protection | Plant Protection | Pesticides | Herbicides | Fungicides | Insecticides | Agriculture | Active Substance | PPP | Phytosanitaire | BioControl | BioPesticide | Biosolutions | BioControle | AIR | CADDY | IUCLID | REACh | CLP