Senior Patent Agent/Counsel (Large Molecule)

Genentech•South San Francisco, CA

73d•Onsite

About The Position

Genentech's Intellectual Property team is seeking a Senior Patent Counsel/Agent with large molecule expertise, including extensive antibody experience. As a partner and business strategist, this individual will push the boundaries of what is possible in a highly competitive industry. This position reports into the Neuroscience & CVRM IP Practice Group in Genentech's Legal Department, but may also support other therapeutic areas and modalities. Come join our passion for creating and leveraging game-changing IP strategies that enable Genentech to "do now what patients need next!"

Requirements

7+ years of patent attorney/agent experience in life sciences patent prosecution, with majority of experience in patent application drafting and prosecution in a pharma/biotech corporate setting and/or representing such clients/matters in a law firm.
Admission to practice before the U.S. Patent and Trademark Office (USPTO) required.
A U.S. law degree (J.D.) and a current "good standing" admission to at least one U.S. state bar is required for attorney applicants.
An advanced degree in biological sciences such as biochemistry, molecular biology, or other areas relevant to biopharmaceutical IP practice.
Demonstrated experience and track record of success in: <li> Building and leveraging global IP portfolios for large molecule biopharmaceuticals at all stages of prosecution and enforcement; <li> Designing and executing complex freedom-to-operate analyses across different technologies and different jurisdictions; <li> Developing and communicating actionable risk mitigation strategies;

Nice To Haves

A Ph.D. is highly desired.
Experience in IP transactions and due diligence is a plus;
Experience in adverse IP proceedings, including but not limited to US litigation, is a plus;
Besides large molecule experience, additional experience with small molecule global IP portfolios at all stages of prosecution and enforcement is a plus;
Experience in gene therapy, cell therapy, and RNA therapeutics is a plus.

Responsibilities

Managing Docket (Patent Preparation and Prosecution)
Driving strategic IP procurement and management of global intellectual property rights for individual large molecule (biopharmaceutical) candidates and products, including drafting and prosecuting patent portfolios, licensing transactions, due diligence assessments, freedom-to-operate, infringement, and validity analyses, and risk evaluation and mitigation strategies.
Managing and prosecuting active global dockets, including handling U.S. and foreign patent applications as well as post-grant proceedings (e.g., reexamination, reissue, post-grant review), including foreign oppositions and appeals, as they may arise.
Rendering due diligence assessments, freedom-to-operate, infringement, and validity analyses, and risk evaluation and mitigation strategies for individual program molecules, technologies, tools, and the like.
Identifying and exploiting new strategic opportunities and approaches by leveraging a deep understanding of patent law and a knowledge of the competitive landscape across the Genentech franchises and portfolio.
Partnering effectively with relevant stakeholders at all levels of the global organization and across all phases of research, drug development, and commercialization to provide clear, strategic business enabling strategies.
Influencing business leaders as a trusted advisor and thought partner.
Deploying in-depth patent and scientific expertise to provide education, guidance, and advice on patent law issues to scientists conducting research and other business stakeholders.
Maintaining and sharing expertise and knowledge on legal case law, rules, or regulations before the U.S. Patent and Trademark Office as well as other relevant jurisdictional IP offices.
Partnering in all intellectual property-related transactions, adverse proceedings, and litigation activities related to individual's program responsibilities.
Participating in group, department, and cross-functional projects and initiatives where strategies, processes, operating standards, and/or practices are developed and deployed to ensure highest quality practices and execution for all aspects of IP portfolios in a high performing, agile team setting.
Sustainably building enduring, productive external relationships with outside counsel, third-party collaborators, and partners.
Ensuring that Genentech remains a great place to practice game-changing IP law, have fun, and make a difference for patients!