Hiring: Senior Corporate Counsel, Global TechOps & Pharma Quality Company: Genentech Location: South San Francisco, CA Job Posted Time: 2026-09-10 11:45:11 Employment Type: Remote Target Skills & Keywords : Risk Management About the job Experience: •7+ years of experience with US FDA/cGMP in a pharma/biotech corporate setting and/or in a law firm or relevant government agency. Required Skills: •Providing strategic legal advice on US FDA facility inspections and foreign health authority inspection as well as internal GMP audits. •Partnering with PT Quality organization to address critical quality issues, supply interruptions, manufacturing deviations, health authority notifications, and field actions. •Advising the External Quality organization responsible for CMO and CDMO oversight to structure novel quality agreements and align on compliance standards for external manufacturing partners and supplier networks. •Managing outside counsel retained to support legal matters. •Communication and Leadership •Pro-active and confident individual who is committed to driving change. •Strong verbal and written communication skills. •Demonstrated capacity to communicate complex and highly technical information clearly and concisely. Qualifications: •A U.S. law degree (J.D.) and current “good standing” admission to at least one U.S. state bar, or be eligible to apply to California’s Registered In-House Counsel program. •Providing manufacturing support in pharmaceutical or biotech industries, such as regulatory counseling on FDA/cGMP related matters. •Strong analytical, written, and oral communication skills in English; proficiency in additional European languages (e.g., German, French, Dutch) is a plus. •Roche’s Genentech’s South San Francisco, California campus (No remote.) •Relocation benefits are not available for this position. Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!