Jobs at Genentech

Lead product strategy and roadmaps for therapeutics discovery tools, bridging wet/dry labs, driving design-make-test-learn solutions, stakeholder alignment, deprecating legacy systems, and enabling data-driven drug discovery.

Lead strategy and execution for organized customers (payers, practice managers, financial decision makers) within Respiratory TA. Develop market/competitive analysis, define customer journeys, align clinical and non-clinical messaging, ensure launch readiness, coordinate cross-functional partners, and drive brand strategy implementation and measurement across channels to advance access and commercial goals.

Develop and apply LC-HRMS and LC-MS/MS methods for metabolomics and lipidomics across biofluids, tissues, and cells. Execute sample preparation protocols, perform mass spectrometry data processing and statistical analysis, build or apply Generative AI workflows, ensure bioanalytical quality control, and collaborate cross-functionally to translate omics data into actionable drug discovery insights.

Manage complex administrative functions for a larger team, including high-level scheduling, project coordination, event planning, financial processes (POs, invoices, accruals), stakeholder relationship management, process improvement, and ownership of projects with minimal supervision.

Lead strategic, scientific, and operational oversight of regulated bioanalysis across nonclinical and clinical development. Drive RBIO vision, CRO partnerships, assay lifecycle management, GxP compliance, and delivery of PK, immunogenicity, and biomarker data. Build organizational capability, implement innovative technologies and operational improvements, steward budgets/resources, and develop leadership talent to support complex modalities and global regulatory submissions.

Genentech's Finance Rotation Development Program is a multi-rotation leadership program exposing participants to Commercial Finance, Technical Operations Finance, R&D Finance, and Controlling & Accounting. Participants receive technical and leadership training, may rotate internationally, and are developed for future finance leadership roles with relocation support and competitive compensation.

Lead translational safety pathology for drug development: design and interpret GLP and investigative studies, perform necropsy/clinical pathology/histopathology, author regulatory/scientific documents, collaborate with toxicologists and in vitro teams, advance digital pathology, mentor staff, and represent the company to regulators and expert groups.

Lead technical ownership of mechanical, electrical, and process/utilities infrastructure across Dixon and SSF sites. Drive capital projects from design through commissioning, implement reliability-centered maintenance, perform RCAs using BAS/CMMS data, and ensure systems meet safety and industry standards for uptime, efficiency, and operational readiness.

The Principal ADS Program Lead oversees data science strategies for clinical programs, ensuring quality, compliance, and effective collaboration across teams, while building talent and promoting innovation.

The role involves strategic leadership for product development in CVRM, focusing on portfolio growth, operational excellence, financial management, and cross-functional collaboration.

Lead development and application of molecular engineering and high-content genomics to discover targets and engineer therapeutics for immune-mediated diseases. Design and execute experiments using CRISPR and other functional genomics tools in primary immune cells and models, integrate NGS/single-cell/proteomic/imaging readouts, collaborate across disciplines, manage multiple projects, and produce publishable results.

Support small-scale and pilot biopharmaceutical manufacturing: operate bioreactors, run pilot studies, lead technical transfers and site investigations, perform process characterization and testing, support equipment commissioning, and collaborate across development and commercial teams to enable process validation and product release.

Design, validate, and run biochemical and cell-based assays to evaluate cardio-metabolic drug candidates. Lead screening campaigns, develop novel assay platforms, implement lab automation, analyze complex data, and communicate results to cross-functional teams to inform candidate selection and mechanism-of-action studies.

Lead enterprise-wide resourcing, workforce planning, and metrics for PDD. Drive budget tracking, forecasting, governance, data quality, and analytics tooling. Build and coach a global team, align headcount and budget to portfolio priorities, and enable executive decision-making through governance, KPIs, and planning systems.

Design, prototype, and scale novel data and AI methods (multi-agent, knowledge graphs, semantic integration) for clinical and real-world data. Build scalable data pipelines, enable low/no-code platforms, collaborate cross-functionally, mentor juniors, and ensure compliance with data privacy regulations (HIPAA, GDPR) while validating proof-of-concepts and supporting analytics projects.

Develop and deploy ML and AI imaging methods into reusable, scalable pipelines and agent-callable workflows for drug development. Collaborate with biology, clinical, and engineering teams to translate biological questions into imaging strategies, validate models for real-world and regulated settings, and integrate multimodal data for actionable insights.

Lead account and contract management within the Kansas/Missouri provider ecosystem, engaging senior financial decision-makers to drive provider contracting, onboarding, and pull-through. Identify partnership opportunities, ensure contract compliance, communicate tier status and formulary implications, and collaborate with internal stakeholders to support commercial objectives and improved patient outcomes.

Serve as the commercial bridge to national and regional therapeutic area experts in malignant hematology, converting TAE insights into strategic, measurable demand-generation and access outcomes. Lead cross-functional alignment, synthesize clinical and competitive intelligence, shape TAE engagement plans across lifecycle, manage compliant fee-for-service activities, and travel extensively to drive advocacy, accelerate product adoption, and influence brand and TA strategy.

Analyze FDA guidances and policy documents; conduct regulatory, policy, and legal research; perform landscape analyses to identify modernization opportunities; monitor policy proposals; coordinate internal communications, workgroups, and project activities; support policy positioning and advocacy; contribute to authoring white papers and guidance comments; engage internal and external stakeholders.

Lead medical writing, editing, and project management for clinical documents (protocols, ICFs, abstracts, manuscripts). Coordinate authoring teams, review cycles, timelines, stakeholder alignment, publishing, and regulatory-compliant documentation. Provide strategic input on protocol design and explore AI tools to optimize workflows.