QC Sr. Associate I (Software Developer Specialist) - Fixed Term GenentechQC Sr. Associate I (Software Developer Specialist) - Fixed TermOceanside, CaliforniaEducational Background: Bachelor’s degree with 8–11 years of experience, a Master’s degree with 6–9 years of experience, or a PhD with 3–6 years of experience in Computer Science (Software Development), Life Sciences (Biology, Biochemistry), or an equivalent combination of education and experience. As a QC Senior Associate I (Software Developer Specialist), you will drive the automation and optimization of digital laboratory processes by designing, creating, and modifying automated workflows and "recipes" within the Biovia software system.
Senior Medical (Science) Director, Neurological Rare Diseases GenentechSenior Medical (Science) Director, Neurological Rare DiseasesIn addition to strong communication skills, this position requires the ability to lead fit-for-purpose teams in a matrix environment, flexibility in prioritizing work, and a mindset to engage in purposeful partnerships to solve complex multi-disciplinary challenges. Experience or relevant knowledge of pre-approval drug development trials and/or post-marketing medical evidence generation, including expertise in controlled and observational study designs, data analysis, and clinical/health economic interpretations.
Field Analytics & Insights Director GenentechField Analytics & Insights DirectorCaliforniaThe Field Analytics & Insights Director is responsible for delivering impactful, data-driven insights that guide key business decisions within a field leadership team (Customer Engagement, Ecosystem, Field Medical, National Access Decision, National Supply & Care Delivery) across the Genentech portfolio. Play an active role in the adoption of analytical products by staying up to date on the product roadmap, participating in training, user testing (as needed), and providing constructive feedback to ensure products are integrated into workflows.
PX Business Designer GenentechPX Business DesignerThe CMG Patient Strategy aims to create a holistic, cross-functional approach to deliver a best-in-class patient experience that aligns with the portfolio, technology tools, and consumer-driven patient expectations in a rapidly evolving business landscape. Public Affairs & Access (PAA) is a multi-disciplinary organization that includes Corporate Communications; Policy, Evidence & Access Strategy; Channel & Contract Management; External Affairs; Patient Experience; and Strategy and Business Operations.
Senior Director, Patient Experience Design GenentechSenior Director, Patient Experience DesignThe CMG Patient Strategy aims to create a holistic, cross-functional approach to deliver a best-in-class patient experience that aligns with the portfolio, technology tools, and consumer-driven patient expectations in a rapidly evolving business landscape. Partner with RDT, DDA, PAA Activation & Capabilities Enablement, Business Designers, and PX Delivery Leaders to validate economic and operational viability, establishing a feedback loop between delivery and design.
Therapeutic Area Manager (TAM), NeuroImmunology - Wisconsin Ecosystem GenentechTherapeutic Area Manager (TAM), NeuroImmunology - Wisconsin EcosystemWisconsinLead end-to-end experience for assigned customers/accounts, driving clinical and non-clinical decision making at the point of care and providing education on topics ranging from clinical to non-clinical aspects. Previous cross-functional industry experience in commercial life sciences (pharma or biotechnology) or related industry engaging with key healthcare ecosystem players (e.g., payers, health systems), is required.
Senior Director, PX Governance GenentechSenior Director, PX GovernanceThe CMG Patient Strategy aims to create a holistic, cross-functional approach to deliver a best-in-class patient experience that aligns with the portfolio, technology tools, and consumer-driven patient expectations in a rapidly evolving business landscape. Public Affairs & Access (PAA) is a multi-disciplinary organization that includes Corporate Communications; Policy, Evidence & Access Strategy; Channel & Contract Management; External Affairs; Patient Experience; and Strategy and Business Operations.
Senior Scientist, Antibody Developability/Biophysics & Portfolio Support, AI for Drug Discovery (AIDD) GenentechSenior Scientist, Antibody Developability/Biophysics & Portfolio Support, AI for Drug Discovery (AIDD)The new Computational Sciences Center of Excellence (CoE) is a strategic, unified group whose goal is to harness the transformative power of data and Artificial Intelligence (AI) to assist our scientists in both pRED and gRED to deliver more innovative and transformative medicines for patients worldwide. Our focus is on translating machine learning models into portfolio impact—working directly with gRED and pRED scientists to apply developability prediction, design optimization, and functional modeling to real projects.
Principal Healthcare Compliance Manager, Healthcare Compliance Office (HCO) Advisory GenentechPrincipal Healthcare Compliance Manager, Healthcare Compliance Office (HCO) Advisory12 or more years of work experience (including 10+ direct experience) in a legal or corporate compliance group in the bio/pharma/DIA industry advising/leading project teams in design, development and implementation of elements of a corporate compliance program or projects with significant organizational impact. You will proactively research evolving regulations, influence the development of long-range plans and overall objectives for Genentech, and represent the department on high-impact cross-functional committees.
Principal Quality Compliance Specialist, CVRM (Holly Springs) GenentechPrincipal Quality Compliance Specialist, CVRM (Holly Springs)Holly Springs, North CarolinaThis plant meets today’s demand for CVRM (Cardiovascular, Renal, and Metabolism) medicines and is scalable to grow with the portfolio, which focuses on next-generation metabolic medicines specifically targeting the global obesity epidemic and Type 2 diabetes. This position is a unique opportunity to embed a robust, risk-oriented Quality Culture into the site's operational design, support a continuous improvement culture, and drive operational excellence, establishing Holly Springs as a center of excellence for aseptic drug product manufacturing.
Rare Blood Disorder Account and Community Manager - RBD-ACM – Upstate NY Ecosystem GenentechRare Blood Disorder Account and Community Manager - RBD-ACM – Upstate NY EcosystemBuffalo, New YorkServe as the primary point of contact and identify opportunities for implementing ecosystem and TA squad strategies in the therapeutic area, engaging with healthcare providers, specialty pharmacies, patients/caregivers, and patient advocacy team members. Strong ability to proactively seek and apply relevant information to solve complex problems, assimilate and effectively communicate clinical and product information, and address operational issues in healthcare product delivery, including reimbursement and supply.
PX Governance & Portfolio Analyst GenentechPX Governance & Portfolio AnalystThe CMG Patient Strategy aims to create a holistic, cross-functional approach to deliver a best-in-class patient experience that aligns with the portfolio, technology tools, and consumer-driven patient expectations in a rapidly evolving business landscape. As the PX Governance & Portfolio Analyst, you will enable effective decision-making across Genentech’s Patient Experience (PX) portfolio by maintaining a consolidated, enterprise-wide view of initiatives, investments, and performance.
Senior Thought Leader Liaison - Neuroimmunology GenentechSenior Thought Leader Liaison - NeuroimmunologyNorth CarolinaThe Senior TLL role at Genentech acts as the lead Commercial enterprise bridge to National & Regional Therapeutic Area Experts (TAEs) across Therapeutic Areas (TAs), operating as a proactive strategic partner who shapes markets and converts TAE influence into measurable results. Actively participate in core Marketing and TLL sub-teams (e.g., ad boards, insights, congresses) and lead cross-functional alignment across Marketing, Medical, CE, Compliance, Legal, and Global teams to focus TLL efforts on key TA and launch needs.
Senior Director, Regional Lead (Midwest Region) GenentechSenior Director, Regional Lead (Midwest Region)Kansas$170,800–$317,300 / yearThe CMG Patient Strategy aims to create a holistic, cross-functional approach to deliver a best-in-class patient experience that aligns with the portfolio, technology tools, and consumer-driven patient expectations in a rapidly evolving business landscape. As the Senior Director, PX Region Lead, you will serve as a strategic regional owner accountable for driving the delivery, performance, and scalable execution of Genentech’s patient support and navigation services across your assigned territory for the entire portfolio.
PX Business Partner (Immunology) GenentechPX Business Partner (Immunology)The CMG Patient Strategy aims to create a holistic, cross-functional approach to deliver a best-in-class patient experience that aligns with the portfolio, technology tools, and consumer-driven patient expectations in a rapidly evolving business landscape. As the Patient Experience Business Partner (PXBP), you will serve as the primary strategic liaison within Patient Experience (PX) for assigned Therapeutic Areas (TAs) to shape, triage, and elevate patient-related strategies and capabilities across Genentech.
Machine Learning Engineer, Infra, AI for Drug Discovery GenentechMachine Learning Engineer, Infra, AI for Drug DiscoveryNew York City, New YorkThe new Computational Sciences Center of Excellence (CoE) is a strategic, unified group whose goal is to harness this transformative power of data and Artificial Intelligence (AI) to assist our scientists in both pRED and gRED to deliver more innovative and transformative medicines for patients worldwide. At Roche’s AI for Drug Discovery (AI4DD) group (Prescient Design), we are building the machine learning platforms that enable researchers and engineers to move models from experimentation into reliable scientific and production workflows.
Lead Clinical Scientist GenentechLead Clinical ScientistGenentech’s Research and Early Development (gRED) Early Clinical Development (ECD) organization is responsible for developing and executing early development clinical strategies and plans to provide proof-of-concept data with respect to safety, efficacy, and the utility of biomarkers for gRED new molecular entities. The Lead Clinical Scientist participates in development of clinical strategies for assigned molecule(s)/indication(s) and is responsible for developing and effective and efficient execution of the Clinical Development Plan (CDP) for one or more molecules.
Scientist 3- Translational Medicine (Multiple Sclerosis & TR focused) GenentechScientist 3- Translational Medicine (Multiple Sclerosis & TR focused)Analyze and interpret high-dimensional datasets from clinical samples, including single-cell RNA-seq, CITE-seq, bulk RNA-seq, spatial transcriptomics, and/or proteomics, to generate translational insights that support clinical development. This role sits at the intersection of clinical development and translational science — the ideal candidate is comfortable working with clinical biospecimens, interpreting high-dimensional datasets, and contributing findings that directly inform clinical trial design and molecule progression.
Principal/Sr. Principal Scientist - Development GenentechPrincipal/Sr. Principal Scientist - DevelopmentThe successful candidate for Principal/Sr Principal Scientist will provide scientific leadership and play an active role in the process of drug development, with a strong emphasis on Genentech’s oncology and cardiovascular, respiratory, and metabolism development project portfolio, which includes small molecules, immunomodulatory biotherapeutics, bi-specific antibodies, ADCs, cancer vaccines and cellular therapeutics. Working in a collaborative team environment, the Principal/Sr Principal Scientist leads the safety assessment of Genentech therapeutics by creating a best-evidence synthesis of existing knowledge and comprehensive investigations of toxicologic activity, strategic planning, and designing/implementing/supervising toxicology studies in support of program advancement.
Principal Customer Operations Oversight Lead (US Medical) GenentechPrincipal Customer Operations Oversight Lead (US Medical)The Principal Customer Operations Oversight Lead plays a pivotal role in driving operational excellence across our US Medical (USM) Contact Center lines of business, including Medical Information, Trial Information Support & Compassionate Use, and Adverse Event Intake. Stakeholder Alignment:Lead seamless collaboration between internal matrix teams and external service providers, taking ownership of complex escalations to ensure timely, stakeholder-aligned resolutions.