Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning.

Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.

*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.

Summary: The Associate Director, Process Validation and Risk Management will lead and facilitate commercial process validation and risk management activities across Vaxcyte’s end-to-end manufacturing processes. This role focuses on technical strategy, execution, and cross-functional coordination to support commercial readiness, regulatory compliance, and lifecycle management. The incumbent will provide leadership to ensure the organization is equipped to effectively design, execute, and communicate process validation and risk management strategies to internal stakeholders, external partners, and regulatory agencies.

This position will report to the Sr. Director of Process Validation within the Global MSAT organization and will collaborate on overall validation strategy, with primary responsibility for process validation execution and risk management frameworks supporting commercial manufacturing. Essential Functions: Process Validation Leadership Provide strategic and scientific leadership for process validation (PPQ, CPV, lifecycle validation) across commercial programs.

Lead and facilitate execution of validation strategies to support technology transfer, site readiness, and product launch. Ensure alignment of validation activities with regulatory expectations and lifecycle management plans. Risk Management Develop and implement risk management frameworks, tools, and processes in collaboration with Quality.

Lead cross-functional risk assessments to identify, evaluate, and mitigate operational, technical, and regulatory risks. Monitor and communicate risk trends and key risk indicators to stakeholders. Commercialization Lifecycle Support Support commercial manufacturing operations by ensuring processes remain in a validated and controlled state.

Contribute to lifecycle management activities, including process improvements and continued process verification. Cross-functional Interface Collaborate with Regulatory, CMC, Quality, Supply Chain, Procurement, and Engineering to support commercialization and supply continuity. Partner with internal teams and external CMOs to ensure alignment on validation and risk strategies.

Technical Oversight Provide guidance for validation of processes, systems, facilities, and methods within the commercial organization. Support deviation investigations, ensuring timely resolution and sustained compliance. Regulatory Contribute to authoring and reviewing regulatory filings and responses to health authorities.

Effectively communicate the scientific and commercial rationale for validation and risk management strategies.