South San Francisco
California, United States of America
Senior Portfolio Manager, Regulatory PMO
The qualified candidate will contribute to the management of the overall PTR portfolio (product and non-product), including portfolio planning and reporting and delivering portfolio analytics and insights to drive operational and business excellence within PTR.
They will partner with the Biologics and Small Molecule platforms to deliver a holistic strategic plan for the Biologics and Small Molecules product portfolio, support portfolio prioritization, resourcing and budgeting processes and facilitate PTR product portfolio reviews as needed. They will work to enhance processes to resource, oversee, track and report on projects within the product and non-product portfolio. In addition, they will drive continuous improvement of the TRT program infrastructure and portfolio management processes in collaboration with external partners such as Pharma Technical Development (PTD), Pharma Technical Supply (PTS), Pharma Development Regulatory (PDR), and other PT or PD functions. The Portfolio Manager will support the knowledge management in PTR by ensuring that critical regulatory information is consistently and easily available to PTR users and partners.
They will take a leadership role in defining, developing and overseeing the execution of a long-range vision, strategy, and plan for the non-product portfolio. They will be a thought partner to the Global Head of Project and Portfolio Management (PPM) and the Regulatory Submission Capability (RSC) Lead/co-chairs on PTR’s non-product portfolio strategic roadmap and portfolio investment decisions. They will drive robust management of PTR’s non-product portfolio by providing a framework for quality decision making, effective resource utilization and enhanced tracking and reporting in the absence of a Central Operations Steering Committee (OSC). They will also own the planning, governance and intake processes for the Non Product Portfolio and oversee the progress of strategic or cross functional projects across multiple PTR or PTx functions. They will provide the RSC Core Team with an objective perspective of PTR’s non-product portfolio to help leverage synergies, solidify, enhance, or transform Regulatory Submission capabilities across PDR and PTR.
Primary Responsibilities and Accountabilities
Education & Experience
A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.
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