Jobs at Intellia Therapeutics

Leads CMC program operations, project planning, risk management, regulatory commitment tracking, dashboards, and executive reporting. Partners cross-functionally across Regulatory, Manufacturing, Quality, Supply Chain, and Process Development teams. Designs and deploys AI-enabled automation, reporting, and risk-flagging tools to improve operational visibility and decision-making. Establishes scalable CMC processes, facilitates meetings, drives follow-through, and supports process improvement and digital transformation across biopharmaceutical programs.

Owns the full contract lifecycle, including drafting, negotiation, execution, and CLM administration. Partners with stakeholders across Research, Clinical, Commercial, and G&A to manage risks and create enforceable agreements. Administers Ironclad workflows, templates, permissions, reporting, and training while improving contracting processes, automation, metrics, and scalability. Supports legal and cross-functional projects in a fast-paced biotech environment.

Conduct discovery proteomics and immunopeptidomics studies to identify biomarkers and characterize immune recognition of genome-editing therapeutic candidates. Responsibilities include sample preparation, LC-MS/MS acquisition, bioinformatic analysis, HLA-presented peptide profiling, assay development, mass spectrometry optimization, technical reporting, SOP authoring, and cross-functional collaboration. The role requires hands-on laboratory expertise in immunopeptidomics, structural and bioanalytical mass spectrometry, and interpretation of complex datasets.

Lead strategy, planning and execution of HCP personal promotion to support commercialization and launch of a gene editing therapy. Develop HCP materials, peer-to-peer and congress programs, manage agency partners, align cross-functionally (Medical, Market Access, Legal, Regulatory), support field training and digital rep-led engagement, and manage Promotional Review Committee processes to drive HCP engagement and product uptake.

Oversee a team applying genomic tools for gene editing therapies, managing projects, budgets, and collaborations to ensure innovative advancements.

Lead QA oversight for QC activities supporting development through commercial manufacture of gene editing products. Provide technical authority on analytical control strategies, method validation/transfers, stability programs, reference standards, investigations, trending/predictive quality, and regulatory inspection readiness. Mentor QA/QC staff and partner cross-functionally to mature QC capabilities for commercial supply.

Lead enterprise QMS strategy and digital compliance for ATMPs and biologics, drive eQMS implementation and CSV, ensure global regulatory and inspection readiness, establish data governance and analytics, manage enterprise risk, and build a high-performing quality organization across clinical to commercial stages.

Manage administration, support, enhancement, and optimization of Veeva commercial and medical platforms. Act as liaison between business, IT, and vendors; translate requirements into technical solutions; lead UAT, impact assessments, process improvements, documentation, and compliance alignment (FDA/HIPAA). Provide technical leadership and oversee incident resolution and integrations.