Job requirements and application form

• Full responsibility for registration, renewal, and label expansion of crop protection products, including biologicals, microbials, biostimulants, and chemical formulations. • Develop and lead regulatory strategies for both the existing portfolio and products under development, aligned with business goals and target markets. • Prepare, manage, and submit regulatory dossiers, including safety, efficacy, quality, manufacturing, and CMC data. • Lead regulatory and field efficacy trials in collaboration with R&D teams, external consultants, CROs, and contractors, locally and internationally. • Serve as the primary interface with regulatory authorities in Israel and abroad, including correspondence management, responses to questions, and handling objections or data gaps. • Continuously monitor regulatory developments and assess their impact on the company’s products and pipeline. • Provide regulatory leadership throughout the product development lifecycle, from concept through commercialization (Regulatory by Design). • Deliver regulatory guidance to marketing and sales teams, including claims substantiation, labeling, and marketing materials. • Manage external consultants, service providers, and regulatory budgets. • Identify, assess, and mitigate regulatory risks, and lead corrective and preventive actions. • Build, lead, and manage the regulatory team, including staff and consultants located internationally. Location: Center District, Israel

• Advanced academic degree (MSc or PhD) in Plant Sciences, Agronomy, Biology, Biotechnology, Chemistry, or a related discipline. • Proven experience in Regulatory Affairs within the pharmaceutical, biotechnology, or life sciences industry, with a strong emphasis on biological products (e.g., biologics, biopharmaceuticals, or microbial-based products). • Experience with international regulatory frameworks (e.g., EU, EPA, OECD or equivalent) is required. • Solid knowledge of microbial products, plant extracts, and biological crop protection solutions is an advantage • Hands-on experience managing field trials and efficacy data, including collaboration with international laboratories and consultants. • Excellent command of English, both written and spoken. • Strong ability to work independently, take ownership, and lead the regulatory function within an entrepreneurial, fast-paced environment. • Demonstrated experience in managing teams, including remote and international teams.