Search the 29 jobs at Genentech

The Senior Device Quality Manager will oversee quality aspects in developing medical devices and combination products, ensuring compliance with regulatory standards. The role entails providing quality engineering leadership, managing internal and external partners, conducting audits, and participating in quality assurance activities throughout the product lifecycle.

This position involves refining the strategy and defining the product vision for gCS Search within the Computational Catalysts group. Responsibilities include managing a team, prioritizing product requirements, conducting market research, and driving the execution of initiatives to enhance scientific productivity through advanced search functionality.

The Data & AI Policy Analyst will define data strategies that comply with international legislation on data collection and analysis. They will collaborate with scientists and policy experts to align computational plans and manage data access, while developing implementation plans to ensure adherence to data policies in the gRED context.

The role involves supporting Manufacturing IT OT systems, participating in system maintenance, validation, and documentation, and coordinating with internal teams on system changes. Responsibilities include user account management and supporting GMP compliance efforts in a highly automated pharmaceutical facility.

The Senior QA Specialist will oversee quality processes for environmental monitoring and aseptic media fill programs within a manufacturing environment. Duties include providing guidance on best practices, supporting validation of facilities, approving environmental control changes, and training staff on aseptic techniques. The role requires collaboration with various departments to ensure compliance with quality standards.

The role involves leading a team in the development of efficient and scalable cell culture processes for biologics, collaborating across functions, training team members, authoring regulatory documents, and influencing technology implementation.

As a Technical Product Manager, you will drive the roadmap for the LLM team, prototype LLM models, coordinate beta-testing, synthesize user feedback into requirements, and work collaboratively with diverse stakeholders on projects involving state-of-the-art LLMs.

The Sr. Supervisor Manufacturing-Bioprocess is responsible for overseeing daily operations, ensuring compliance with cGMP standards, managing staff development, implementing continuous improvement projects, and maintaining a safe manufacturing environment for GMP products.

The Principal Software Engineer will design and lead the development of Genentech’s Lab-in-the-Loop AI platform for drug design, manage a team of software engineers, and create integrated web applications while collaborating across several teams.

The Enterprise Data Architect will lead the design and implementation of a federated data architecture for Genentech's research organization, ensuring data is effectively structured and integrated into applications. This role emphasizes collaboration with scientists and data engineers, establishing data governance, quality standards, and driving innovative data solutions for AI/ML activities.

The Senior Program Manager will manage the Digital Performance Management tool, drive data analysis, and work with machine learning models to enhance business performance. Responsibilities include overseeing performance reviews, developing visual dashboards, automating data processes, collaborating with cross-functional teams, and implementing continuous improvement initiatives.

The Site Technical Transfer and Launch Lead is responsible for the planning, coordination, and execution of tech transfers and new product launches within the Parenteral Launch and New Technology team. This role involves managing project teams, resource planning, and ensuring compliance with regulatory standards while fostering collaboration across local and global partners.

The Research Associate 2 conducts laboratory experiments and scientific activities to support projects at Ventana. Responsibilities include designing experimental protocols, analyzing data, preparing technical reports, and maintaining laboratory documentation. The role necessitates teamwork, creative problem-solving, and continuous quality monitoring in a GMP/GLP environment.

The Commercial Rotational Development Program at Genentech offers a three-year rotational experience in key commercial roles related to healthcare and biotech. Participants will engage in both field and home office rotations, gaining skills necessary for success in the biotech/pharmaceutical industries while receiving mentorship and training.

The Head of Finance for Site Operations will provide strategic decision support and budget management for G&A functions. Responsibilities include guiding capital projects, managing monthly and quarterly financial deliverables, fostering a collaborative team environment, and enhancing budgeting processes. This role requires significant experience in finance and the ability to influence senior management.

As a Quality Control Associate, you will establish and execute analytical testing processes to enable the manufacturing of cell and gene therapies while ensuring regulatory compliance. Responsibilities include performing analytical testing, conducting assay transfer, technical data review, writing documentation, supporting audits, and participating in project teams.

The System Process Engineer will provide 24x7 support for applications, specifically SAP R3 and ASPIRE S4/EWM, support continuous improvement initiatives, conduct user training, and serve as the liaison between end-users and IT teams. Responsibilities include troubleshooting, monitoring system interfaces, and facilitating process improvements in a biotech setting.

As a Principal Automation Engineer at Roche, you will lead automation efforts including commissioning and qualifying new systems, troubleshooting complex automation issues, and collaborating with cross-functional teams to enhance operational performance. Your role also involves supporting junior engineers and improving documentation practices.

The Systems Process Engineer will support, improve, and onboard digital manufacturing processes, acting as a liaison between end-users and IT applications. Responsibilities include troubleshooting applications, leading continuous improvement initiatives, and conducting end-user training, primarily focused on SAP systems. The role requires a strong understanding of IT and process improvement in biopharma environments.

The Technical Lead will oversee Quality Control operations, ensuring compliance and process standardization through investigations, corrective actions, and documentation. Responsibilities include leading cross-functional teams, developing CAPAs, guiding less experienced colleagues, and managing quality compliance documentation. The role also involves direct material release and participation in project teams for system implementation.