Jobs at Artiva Biotherapeutics

Conduct translational research and biomarker analysis supporting autoimmune disease clinical trials. Develop and run immunophenotyping, cytotoxicity, proliferation, and cytokine assays; perform flow cytometry QC; analyze clinical biospecimens and report findings. Collaborate with Clinical Operations, Clinical Development, and Data Management on biomarker strategy, sample logistics, and trial data interpretation. Present results, support publications, maintain compliant laboratory documentation, and follow protocols and safety procedures.

Support enterprise IT systems, infrastructure, laboratory applications, business platforms, and end users in a regulated biopharmaceutical environment. Responsibilities include SOX and GxP compliance support, ERP and business application administration, helpdesk and onboarding services, Microsoft 365 and identity administration, infrastructure maintenance, backup and disaster recovery, asset procurement, vulnerability remediation, automation, and inspection readiness activities.

Conduct analytical testing supporting process development of allogeneic NK cell therapies. Responsibilities include in vitro assays, data analysis and trending, assay transfers, troubleshooting, technical documentation, cross-functional coordination, and training personnel on analytical procedures. The role requires hands-on experience with flow cytometry, plate readers, automated cell counters, and relevant laboratory experience in biological sciences, with cell therapy, immunology, oncology, and regulated GxP experience preferred.

The Senior Director, Safety and Pharmacovigilance leads Safety and PV activities, ensuring compliance with regulations, overseeing adverse event reporting, and managing vendor relationships.

Lead MSAT technical support for allogeneic clinical and commercial manufacturing: execute tech transfers, author batch records and SOPs, qualify equipment (IQ/OQ/PQ), perform process validation, troubleshoot production, manage deviations/investigations and CAPA, support raw material/E&L assessment, create manufacturing dashboards, and establish track-and-trend programs with biostatistics.

The Senior Associate, QA Compliance is responsible for overseeing quality assurance compliance, managing deviations, CAPAs, change controls, and supporting audits in an FDA regulated environment.

Lead strategic direction for cell potency analytical development, design and validate cell-based assays for NK cell therapies, mentor scientists, author SOPs and regulatory sections, manage assay transfers to QC, and collaborate with R&D and Process Development to support product characterization, release, and stability.

Develop, optimize, and validate flow cytometry and cell-based potency assays to characterize and support release of allogeneic NK cell therapies. Execute benchtop experiments, draft SOPs/protocols/reports, collaborate with R&D, Process Development, and QC, and support assay transfer and qualification/validation in a regulated environment.

Lead and execute operational aspects of clinical/translational biomarker programs: manage central lab/CRO relationships, kit logistics, sample tracking, assay documentation, budgets/contracts, team leadership, and coordination with Clinical Operations and Translational Science to ensure timely, high-quality biomarker data delivery.

Lead and build GMP Quality Assurance for internal cell therapy manufacturing: own quality systems (deviations, CAPA, change control, batch disposition), inspection readiness, and BLA/CMC quality preparedness. Partner with Technical Operations and Regulatory Affairs, drive risk-based decisions, chair quality governance, and manage a GMP QA team to ensure compliance with FDA/EMA/ICH standards and continuous improvement.