Senior Manager / Associate Director, Regulatory Affairs CMC (Small Molecules)

Senior Manager / Associate Director, Regulatory Affairs CMC (Small Molecules)Shape the CMC regulatory path for Nurix's small molecule portfolio, from clinical development through marketed lifecycle. You'll combine hands-on authoring of Module 3 (Quality) content with real strategic influence as the CMC regulatory voice on cross-functional teams, with room at the Associate Director level to own strategy and mentor junior regulatory staff.The OpportunityReport to the Senior Director, Regulatory Affairs CMC (Head of Regulatory CMC, Small Molecules) as a key member of the Regulatory Affairs teamDevelop, communicate, and execute global CMC regulatory strategies for assigned programs (drug substance and drug product) across the product lifecycleAuthor, review, and compile high-quality CMC (Module 3 / Quality) content for regulatory submissions, including IND/IMPD and equivalent global filings, amendments, annual reports, and responses to health authority questionsAssess the regulatory impact of manufacturing, analytical, formulation, and supply chain changes, and recommend filing strategies and categorization (e.g., substantial, non-substantial, annual reportable)Provide proactive CMC regulatory guidance and risk assessment to development, technical operations, and commercial teamsPartner with Technical Operations/Manufacturing, Analytical Development, Quality Control, Quality Assurance, Supply Chain, and CMOs/CDMOs (where applicable) to align technical activities with regulatory requirementsRepresent CMC Regulatory on project and CMC sub-teams, and manage submission timelines and deliverables in coordination with regulatory operations and publishingEnsure submission content is accurate, consistent, scientifically sound, and compliant with ICH guidelines and regional requirements (FDA, EMA, and other markets relevant to the portfolio)Contribute to regulatory intelligence by monitoring evolving guidance and precedent and translating it into practical adviceOversee quality assurance processes to ensure compliance with regulatory standards, and participate in cross-functional initiatives that improve regulatory submission processes and systemsAt the Associate Director level, take greater strategic ownership and, where applicable, provide line management or mentoring of junior regulatory staffWhat You'll BringBachelor's degree in chemistry, pharmacy, pharmaceutical sciences, chemical engineering, or a related life sciences field is required; an advanced degree (M.S., Ph.D., or Pharm.D.) is preferredMinimum 6+ years in regulatory affairs with a substantial focus on CMC, and 10+ years of overall pharmaceutical/biotech industry experienceDemonstrated experience authoring and/or compiling CMC (Module 3) content for regulatory submissions for small molecule productsWorking knowledge of ICH quality guidelines and of FDA and/or EMA CMC requirements; familiarity with other global regions is a plusSolid understanding of pharmaceutical development, manufacturing processes, and analytical methods for small moleculesStrong written communication and scientific/technical writing skillsAbility to manage multiple projects and competing timelines with attention to detailEffective cross-functional collaboration and stakeholder managementComfort operating with autonomy while escalating appropriatelySalary Range: $187,800 - $208,600The posted range applies to roles based in the San Francisco Bay Area and reflects local market conditions. Where an offer lands within that range depends on the candidate's relevant experience, technical expertise, and how their background aligns with the role's requirements.Location: Onsite – Brisbane, CAFit with Nurix Culture and ValuesStrong team orientation; highly collaborativeSolutions and results-oriented focusHands-on approach; resourceful and open to diverse points of viewAbout Nurix TherapeuticsNurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.