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The Senior Scientist will develop and optimize upstream processes for polysaccharide manufacturing, lead and mentor junior staff, and collaborate with cross-functional teams. Responsibilities include designing and executing experiments, optimizing fermentation parameters, implementing new technologies, and preparing technical documents and reports.

The Scientist I in Conjugation Development will develop processes for the company's pneumococcal conjugate vaccine, focusing on synthesis, purification, and analytical characterization of polysaccharides and conjugates. Duties include optimizing multi-step syntheses, purifying compounds using various methods, analyzing results, maintaining records, and tracking inventory in a lab setting.

The Contracts Administration & Technology Specialist will oversee Vaxcyte’s contract management system, manage legal agreement intake, optimize the legal contract repository, educate users on Ironclad functionalities, and support compliance and administrative efforts in the Legal Department. The role also involves collaboration with attorneys, management of contracts, and reporting activities.

The Associate Director of Accounting will lead accounting operations, supervise monthly close processes, manage balance sheet accounts and implement process improvements. The role requires collaboration within the finance team and leadership to ensure compliance and efficient operation.

The Sr. Director of Quality Assurance and Compliance at Vaxcyte will ensure inspection readiness and regulatory compliance. Responsibilities include managing vendor programs, overseeing audits, establishing compliance processes, monitoring regulations, leading quality initiatives, and promoting a quality mindset throughout the organization.

The Payroll Manager at Vaxcyte will oversee all payroll processes, maintaining compliance with tax laws and company policies, and facilitating employee onboarding and offboarding. Duties include payroll preparation, tax withholding management, participation in month-end close processes, and automation of payroll and stock administration processes for efficiency. The role also involves employee education and collaboration on projects related to accounting and regulatory audits.

The Associate Director of Quality Control will manage global reference standards and critical reagents, ensuring compliance with ICH guidelines. They will lead policy development, oversee technical documentation, and collaborate with CMC, QA, and RA teams for clinical and commercial product testing and release.