Associate Director, Immunoassay Critical Reagents and Reference Materials

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.

• 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
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  Everyone leads at Vaxcyte with a kindness‑first, inclusive approach to collaboration and vigorous debate that advances our business objectives.
• MODEL EXCELLENCE
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  The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.

Vaxcyte is seeking an accomplished Associate Director, Immunoassay Critical Reagents and Reference Materials to join the Global Analytical Development organization. This role will provide scientific and strategic leadership for the development, qualification, characterization, governance, and lifecycle management of critical reagents and reference materials that support immunoassays across Vaxcyte's vaccine pipeline.

This is an onsite, laboratory‑based scientific leadership position requiring active engagement in laboratory operations, study oversight, inventory management, data review, and technical decision‑making. The successful candidate will bring deep expertise in antibody generation and characterization, reagent qualification, reference standard development, customized assay material management, stability assessment, and lifecycle strategy.

A key focus of this role will be establishing and maintaining robust reagent and reference material systems that ensure long‑term supply continuity, analytical reliability, and regulatory readiness. The individual will support immunoassay platform advancement and enable fit‑for‑purpose assays throughout development, validation, commercialization, and lifecycle management.

The Associate Director will collaborate closely with cross‑functional teams, including Analytical Development, Quality, Manufacturing, Regulatory Affairs, and Supply Chain, as well as external partners such as CROs, CDMOs, contract testing laboratories, reagent suppliers, and technology providers. This role is responsible for ensuring the consistent availability, performance, documentation, and oversight of critical immunoassay materials while driving continuous improvement and operational excellence across the portfolio.

• Contribute to the establishment and growth of the Immunoassay Development Capability within Global Analytical Development organization, with primary responsibility for immunoassay critical reagents, reference materials, customized assay materials, stability programs, and associated lifecycle management systems.
• Engage daily in laboratory operations, including reagent planning, reference material planning, sample and material readiness, laboratory study coordination, inventory review, data review, documentation, and hands‑on technical support.
• Lead the generation, characterization, qualification, stability planning, lifecycle management, and inventory control of antibody reagents used in immunoassays, including capture antibodies, detection antibodies, monoclonal antibodies, polyclonal antibodies, labeled antibodies, and other assay‑specific binding reagents.
• Support antibody reagent generation strategies, including antigen design, immunization strategy, hybridoma or recombinant antibody generation, screening, clone selection, purification, conjugation, labeling, characterization, and long‑term supply planning.
• Develop and execute antibody characterization plans, including specificity, affinity,…