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knoell

Your go-to partner for global regulatory registration!

Senior Regulatory Affairs Manager

Account ManagerSalesPart TimeRemoteLeadTeam 501-1,000Since 1996H1B No SponsorCompany SiteLinkedIn

Location

Northern America

Posted

2 days ago

Salary

0

Seniority

Lead

No structured requirement data.

Job Description

Senior Regulatory Affairs Manager

knoell

Role Description knoell is seeking an experienced Senior Manager of Regulatory Affairs to join our North American team in a part-time capacity (16-20 total hours across 4 business days weekly). This position is designed for a seasoned professional who thrives at the intersection of science, regulation, and client strategy. - Serve as a regulatory expert for registering products across crop protection, biologicals, and antimicrobials/biocides. - Collaborate closely with the local knoell USA team and global network of experts to ensure seamless service delivery for clients’ critical registration and regulatory strategy projects. - Mentor other colleagues in developing regulatory expertise. - Act as the “go-to” expert for EPA FIFRA pathways, providing support from data gap analysis to final label approval. Qualifications - Bachelor’s degree required in Biology, Chemistry, Toxicology, Natural Resources, or a related scientific discipline. (Advanced degree preferred.) - Minimum of 8+ years of professional experience in the registration of agrochemicals, crop nutrition, or related fields at the U.S. federal level. (Additional international regulatory expertise preferred.) - Proven track record of successfully registering products under FIFRA, including deep familiarity with regulatory strategy, data requirements, and risk assessment frameworks. - Exceptional written and verbal communication skills in English; able to translate complex regulatory concepts for diverse audiences. Requirements - Expert knowledge of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) to register traditional actives, “me-too” products, biopesticides, and antimicrobial/biocide products. - Navigate the unique regulatory landscapes for biologicals (biopesticides, biostimulants, microbials), leveraging recent regulatory developments to accelerate time-to-market. - Perform comprehensive data gap analyses, draft waiver requests, and design testing strategies to meet EPA and state-level requirements. - Draft and review regulatory labels including those for biological products, identifying issues and ensuring compliance with federal and state labeling laws. - Act as a primary point of contact for the knoell team for North America expertise, contributing to education of the team on regulatory pathways, risks, and opportunities. - Provide expertise alongside project managers in initial client inquiry calls, collaborate with internal sales teams on client proposals and quotes, and advise on budget needs based on project scope and complexity. - Provide competitive intelligence and insights into emerging regulatory trends (e.g., new state-level regulations, EPA policy shifts). - Work closely with global colleagues to align North American strategies with international frameworks (JMPR, EU, etc.). Benefits - Opportunity to work in a dynamic family-owned business environment with an international team. - Development opportunities to support personal, leadership, and technical development, including English language courses. - Flexible working policy and remote-first company culture. - Part-time work options generally supported on request. - Celebration of work-life balance for colleagues. - Global employee referral program with rewards for referring talent to knoell.

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