Jobs at Genentech

Lead human factors activities for combination products and drug delivery devices: plan and run ethnographic and usability studies, perform use-related risk analysis (uFMEA), author protocols and reports, develop IFUs and training materials, translate user needs into engineering requirements, and analyze qualitative/quantitative data to drive user-centered design.

The Portfolio Leader in Oncology will develop strategies, manage the portfolio, support decision-making, and communicate insights to influence portfolio decisions in the Therapeutic Area.

Lead end-to-end technology transfer for clinical drug substance manufacturing, ensure regulatory and GMP compliance, coach and mentor teams, drive standardization and continuous improvement, and collaborate cross-functionally to optimize throughput and reduce lead times.

Contribute statistical expertise to design, conduct, analysis, and interpretation of clinical trials. Draft protocols and SAPs, perform analyses, support regulatory submissions, represent Biostatistics on study teams, summarize findings, and apply established methods with guidance to ensure scientific rigor and regulatory compliance.

The Senior Thought Leader Liaison coordinates between therapeutic area experts and commercial strategies, influencing market perceptions and driving demand for products through engagement and education. Responsibilities include managing relationships, translating insights into strategies, and enhancing patient access to therapies.

Lead the development of measurement products, managing product roadmaps, stakeholder engagement, and ensuring compliance while driving product experimentation and optimization.

Lead the Controllers Group transformation and digital initiatives as the Federated Digital Champion. Manage a PMO portfolio, roadmap, governance, project delivery (including UAT), change management, and value realization. Coordinate with Digital Finance, global teams, and stakeholders to drive adoption, track adoption metrics, and identify next-wave opportunities to advance self-service and automation.

Lead and coach a Boston-based team of Operations Partners while remaining hands-on delivering complex executive administrative support to senior leaders. Oversee calendar and travel logistics, events, expense processing, and cross-timezone coordination; partner with cross-functional teams and drive local alignment with global practices and process improvements using digital and AI-enabled tools.

Field-based account and community manager for rare blood disorders responsible for engaging HCPs, specialty pharmacies, patients/caregivers, and advocacy groups. Drive local execution of national strategy, deliver product education per FDA guidelines, identify and solve complex account needs, mobilize cross-functional experts, and support patient access, reimbursement, and care navigation to improve outcomes and lower costs.

Lead development and execution of functional pharmacology assays using iPSC-derived and organoid models to characterize large-molecule candidates. Drive candidate selection across disease indications, design high-throughput workflows with automation and bioinformatics, collaborate cross-functionally, manage CRO/vendor studies, and present data to project teams and leadership to inform decision-making.

Lead cross-functional Technical Development Teams to define and execute CMC strategies for large‑molecule drug candidates from early trials through launch. Drive manufacturing, drug product/device, supply chain, regulatory planning, risk mitigation, resourcing, and program delivery while advising senior leadership and ensuring timely, compliant development and clinical supply supply execution.

The Senior/Principal Engineering Standards Steward drives technical standards, regulatory compliance, and efficiency in engineering projects while collaborating with teams and managing standards lifecycle.

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 Executive Director of Portfolio Insights & Analytics leads insights, analytics, and measurement strategy for business decisions, managing a high-performing team to leverage data and technology.

Responsible for overseeing Raw Materials and Equipment Qualification programs in Quality Control, ensuring compliance with GxP standards and continuous operational improvement.

The Expert Data Scientist develops advanced data visualizations and analytics, drives automation and AI integration, and collaborates with stakeholders on data review processes in clinical development.

Lead cross-functional, country-level rollout of advanced CRM and portal capabilities to unify legacy applications into a cohesive digital ecosystem for clinical site identification, setup, and engagement. Define vision and roadmaps, manage multiple workstreams, drive stakeholder alignment across Clinical Operations and CROs, and scale piloted solutions to improve site activation, budgeting, contracts, and site engagement workflows.

The Immunotherapy Specialist I will assist in manufacturing cell and gene therapies, ensuring compliance with SOPs, conducting training, and performing environmental monitoring in cleanrooms.

Support PTQ Quality Processes by contributing to initiatives, facilitating workshops, developing metrics and data repositories, generating business insights, and assisting PTQ strategy and project management across cross-functional teams.

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.