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Develop, maintain, and productionize reproducible, scalable analytical workflows and tools for bulk and single-cell transcriptomic and epigenetic data. Collaborate with computational scientists to convert analyses into reusable components, integrate multimodal data formats, and provide interfaces for scientists and downstream systems.

Lead Genentech SSF Site Services digital transformation by defining and executing a global digital strategy, managing digital product portfolio and roadmaps, coaching digital leads, partnering with IT and global digital teams, driving adoption of data-driven tools and measuring impact to improve operational efficiency.

The Technical Development Principal Engineer oversees drug product process designs, leads technology transfers, and collaborates with cross-functional teams to develop and validate pharmaceutical processes.

The Principal Project Controls Engineer monitors CAPEX projects' financials, oversees scheduling, conducts analyses, and ensures compliance with financial standards while collaborating with cross-functional teams.

The Senior Principal Statistician leads statistical strategies in clinical trials, ensuring scientific rigor and regulatory compliance while mentoring junior staff and contributing to drug development.

Lead advanced analytical initiatives to optimize pharmaceutical distribution processes using data science methodologies. Design predictive models, analyze data, and present strategic insights to senior leadership.

The Analytical Data Science Lead guides technical strategy and operational execution for multiple clinical programs, ensuring high-quality and regulatory-compliant analytical outputs, while managing a team of programmers and fostering innovation.

The role involves finalizing process equipment design, ensuring operational readiness, managing technical specifications, and collaborating with teams for successful technology deployment and operational standards in sterile drug product manufacturing.

The Principal Quality Control Specialist will oversee QC Master Data management in a GMP setting, lead investigations, develop training, and ensure compliance with quality standards.

The Principal Biostatistician designs and analyzes early-phase clinical trials, applying statistical expertise to inform trial strategy and regulatory interactions. Responsibilities include leading study designs, ensuring quality statistical deliverables, and shaping clinical narratives based on complex data analysis.