Associate Director, Drug Substance Manufacturing – Upstream Process

Vera Therapeutics is a commercial-stage biotechnology company focused on the pursuit of truth in science to transform medicine in autoimmune disease, starting with the kidney. Vera Therapeutics’ flagship commercial product is TRUTAKNATM (atacicept-vymj), a B-cell activating factor (BAFF) and A proliferation-inducing ligand ( APRIL) inhibitor. Vera Therapeutics is evaluating multiple diseases where the reduction of autoantibodies through inhibition of BAFF and APRIL may prove clinically meaningful. Vera Therapeutics was founded in 2016 and is based in Brisbane, California. To learn more, visit www.veratx.com . At Vera, our values are the cornerstone of our culture and guide how we work together every day. We lead with empathy, act with an owner’s mindset, demand clarity, work without fences, and execute with urgency because patients are counting on us. From how we hire and develop our people to how we advance rigorous science, we are building a team committed to transforming medicine in autoimmune diseases, starting with the kidney. Position Summary: The Associate Director, Drug Substance Manufacturing – Upstream Process will report to the VP, Commercial Manufacturing Operations and will be responsible all aspects of Drug Substance (DS) biologics manufacturing with expertise in upstream processing. The individual will serve as a subject matter expert (SME) in upstream processes for outsourced drug-substance manufacturing, technology transfer, life cycle management, and global regulatory submissions of complex Biologics, monoclonal antibodies, and other recombinant therapeutics. Working with the CMC team and other key functions such as project management, QA and Regulatory, the ideal candidate must be an outstanding leader with a proven track record of overseeing all drug-substance upstream manufacturing activities at the CMO site, including process scale-up, technology transfers, validations, PPQ campaign support, continuous process improvements, and post-approval lifecycle management of commercially approved products. In addition, the role requires authoring, reviewing, and editing of CMC related regulatory submissions (e.g., BLA, MAA) and associated quality documents. The candidate must have exceptional organizational and communication skills, be capable of communicating strategic plans to upper management, summarize data, and effectively manage interactions with stakeholders across functions. Responsibilities: Technical Oversight & Manufacturing Support Serve as primary technical interface with global CMOs supporting Drug Substance manufacturing upstream activities. Lead investigations for technical deviations, root cause analyses, and CAPA implementation. Supervise campaign readiness, change management, and process optimization discussions. Lead internal technical meetings and contribute to managing timelines, supply impact, risks, and budget. Technology Transfer & Validation Oversee technology transfer and process qualification across CMO sites. Author and review validation protocols, reports, and technical documentation. Drive continuous improvement initiatives across upstream processes. Drive industry benchmarking and knowledge-sharing across teams. Lifecycle Management & CPV Perform statistical analysis on campaign data to create and analyze process trends and control charts. Develop near-term and long-term lifecycle management / process improvement strategies. Facilitate execution utilizing digital tools (e.g., big data modelling tools), as applicable, for commercial products across manufacturing sites. Establish and maintain robust process monitoring and Continuous Process Verification (CPV) protocols /procedures. CMC & Regulatory Support Author and review CMC sections for global regulatory submissions (NDA, BLA, MAA). Support filing in new markets and conduct impact assessment to post‑approval changes. Support responses to health authority questions related to manufacturing processes and controls. Ensure manufacturi…