Jobs at Genentech

Lead translational safety pathology for multiple drug-development programs from discovery through regulatory milestones. Interpret necropsy, clinical pathology, and histopathology findings; integrate toxicology, pharmacology, translational, and clinical data; guide risk assessment, dose selection, study design, and regulatory strategy. Lead investigative studies, biomarkers, digital pathology, and innovative nonclinical methods. Author regulatory materials, engage health authorities, mentor scientists, and provide cross-functional scientific leadership.

Leads customer marketing strategy, omnichannel campaign development, compliant content creation, agency management, field deployment, and performance optimization for Genentech’s upcoming MASH metabolic disease launches. Focuses primarily on healthcare professionals, with some patient marketing, while partnering across commercial, medical, global, access, legal, regulatory, and external affairs teams. Develops customer insights, positioning, measurement plans, campaign tactics, and integrated experiences to drive customer and business outcomes.

Two-year early talent program providing foundational experience in pharmaceutical regulatory affairs. Participants support regulatory projects, prepare scientific and regulatory documents, assist with Health Authority interactions, collaborate with global drug development teams, and learn across therapeutic areas and product lifecycle stages. The role is based on-site in South San Francisco and is designed for recent life sciences graduates with limited pharmaceutical experience.

Develop and implement measurement strategies, KPIs, and frameworks to evaluate strategic investments and initiatives. Analyze data, identify optimization opportunities, conduct benchmarking, and provide guidance on data sources and measurement methods. Create visualizations, reports, and presentations that communicate insights and recommendations to stakeholders. Collaborate cross-functionally, support data-driven decision-making, and identify opportunities to automate and scale measurement processes.

Owns the roadmap and delivery of media and social operations products, including campaign setup, asset trafficking, social listening, media QA automation, and operational insights. The role translates marketing and agency workflows into scalable self-serve tools, partners with technology and analytics teams, defines requirements and success metrics, and ensures compliance. It requires strong product management experience in martech, adtech, media operations, and digital media platforms.

Leads an antibody engineering laboratory team developing innovative protein technologies and next-generation biotherapeutic formats. Directs bench research, develops predictive assays, defines molecular requirements, advances therapeutic candidates, and collaborates across biology, structural science, translational research, and technical development. Builds an inclusive, high-performing scientific culture while translating protein engineering and biological discoveries into medicines.

Leads the strategic application of medical imaging across Roche’s cardiovascular, renal, and metabolism drug development pipeline. Defines scalable, regulatory-ready imaging endpoints and roadmaps; applies AI, machine learning, and advanced analytics; oversees imaging algorithms from assessment through deployment; and drives global cross-functional initiatives, governance, partnerships, and data standardization.

Leads enterprise-scale digital product delivery for laboratory automation and AI-enabled workflows in pharmaceutical R&D. Owns product roadmaps, domain strategy, cross-functional Agile delivery, executive stakeholder engagement, and complex problem solving. Shapes strategic capabilities, mentors colleagues, scales Agile frameworks across product squads, and guides innovation in lab digitalization, scientific workflows, and AI-ready datasets.

Leads strategic planning, resource allocation, budgeting, operational strategy, and execution for Early Clinical Development. Advises leadership, facilitates meetings, tracks actions, drives talent and engagement initiatives, coordinates cross-functional stakeholders, manages change, and resolves complex business challenges. Requires regular onsite presence in South San Francisco, extended working hours as needed, and domestic and international travel.

Design, deploy, and optimize production generative AI agents and agentic workflows for enterprise applications. Responsibilities include tool schemas, APIs, orchestration, RAG, memory, evaluation, observability, guardrails, security, and human-in-the-loop escalation. The role partners with engineers and business product owners to integrate reliable GenAI systems across regulated commercial, medical, and government affairs environments.

Leads complex change initiatives and commercial capability transformations within Public Affairs & Access. Responsibilities include onboarding brand teams, designing tailored training, coaching champion networks, optimizing workflows, partnering cross-functionally, tracking engagement adoption, and facilitating workshops. Requires strong commercial experience, strategic ownership, project management, communication, and change leadership skills in pharmaceutical, biotech, managed care, or related environments.

Owns strategy, roadmap, requirements, governance, and operational oversight for territory and roster management products. Partners with business stakeholders and engineering teams to optimize territory assignments, roster management, talent-flow insights, data quality, and integrations. Leads product adoption, change management, UAT, reporting, stakeholder alignment, and business-value measurement across a regulated healthcare organization.

Lead development and productization of advanced statistical and ML solutions for clinical development. Design simulation studies, build scalable data and model pipelines, ensure model fairness/compliance, integrate models into product platforms, and drive scientific leadership and cross-functional initiatives in regulated pharma environments.

Conducts microbiological and chemical testing of manufacturing environments and commercial products, performs equipment calibration and troubleshooting, investigates laboratory issues, maintains compliance with cGMP and GLP, prepares analytical reports, updates procedures, and supports data review, training, and cross-functional QC activities.

Field-based Account Executive responsible for selling centralized diagnostic capital and consumable solutions, managing hospital customers, expanding Roche partnerships, identifying new opportunities, closing sales, and meeting territory quotas. The role includes account management, contracting, negotiation, problem solving, project coordination, presentations, strategic planning, and cross-functional collaboration in a regulated environment. Overnight travel is required as needed throughout the Indianapolis territory.

The posting provides no specific responsibilities or qualifications beyond the Quality Control Associate I title and Genentech’s equal opportunity and applicant accommodation statements.

Designs scalable omnichannel architecture for Genentech, including customer data, identity, integrations, segmentation, personalization, orchestration, activation, and analytics. Leads Adobe Experience Platform architecture across RT-CDP, Journey Optimizer, and Customer Journey Analytics. Establishes data models, integration patterns, governance, privacy, security, and compliance standards while guiding product, engineering, data, business, and vendor teams. Defines the architecture roadmap, evaluates technologies, manages risks, and translates business needs into sustainable technical solutions.

Develop human iPSC-derived retinal models and cell-based assays to identify and validate therapeutic targets for AMD and other retinal diseases. Design experiments, investigate disease mechanisms, evaluate therapeutic candidates, maintain rigorous records, and ensure reproducible data. Collaborate across multidisciplinary research teams, adopt new analytical and experimental workflows, and communicate findings internally and at scientific conferences.

Supports Rockwell PharmaSuite MES recipe authoring, software development, validation, troubleshooting, and integration within a 24/7 GMP pharmaceutical manufacturing environment. Develops test plans, supports technology transfers, batch review and release, automation and business-system integration, and MES standards. Consults with process owners, manages changes and deviations, documents incidents, contributes to projects and optimization initiatives, presents electronic batch-record processes to health authorities, and participates in monthly after-hours on-call support.

Leads centralized business operations for a 40-person Public Affairs and Access department. Oversees strategy, planning, budgeting, operational execution, business continuity, compliance support, change management, communications, and organizational development. Partners with senior executives and functional vice presidents, manages managers and individual contributors, and drives cross-functional alignment, enterprise strategy, and high-performing team development.