Manager/Sr. Manager, Training and Doc Control Support Systems

Role: Document Control & Training Manager overseeing document management and training processes within a biopharma environment. Responsibilities: lead document control compliance, improve processes, manage electronic documentation systems (Veeva QualityDocs, Veeva Training), coordinate document updates, review change controls, manage training roles and curricula, and support audits and inspections. Qualifications: bachelor’s degree; 5-10 years in a pharmaceutical QA role; experience with EDMS/LMS, especially Veeva; in-depth knowledge of GxP regulations and Good Documentation Practices; strong organizational and technical writing skills; ability to work independently in a fast-paced setting. HighValue: focus on quality systems, document management, training within a biopharma context, supporting GxP compliance, and audit readiness. WorkSetup: hybrid in San Francisco, in-office 2-3 days/week.