
201 - 500 employees
Founded 2013
đ„ Healthcare
đ Manufacturing
đ§Ź Biotechnology
Healthcare âą Manufacturing âą Biotechnology
Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to prevent and treat serious bacterial infections. The company develops broad-spectrum conjugate and novel protein vaccinesâusing modern synthetic chemistry and a proprietary cell-free protein synthesis platform licensed from Sutro Biopharmaâto create difficult-to-make protein antigens more efficiently. Its lead programs are pneumococcal conjugate vaccine candidates VAX-31 (31-valent) and VAX-24 (24-valent) in Phase 2/3 studies, with earlier-stage candidates targeting Group A Strep and Shigella; Vaxcyte focuses on reducing invasive bacterial disease burden, antibiotic resistance consequences, and related morbidity in vulnerable populations.
đ June 25
đ California â Remote
đ” $174k - $203k / year
â° Full Time
đŽ Lead
đ Director
đŠ H1B Visa Sponsor
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201 - 500 employees
Founded 2013
đ„ Healthcare
đ Manufacturing
đ§Ź Biotechnology
Healthcare âą Manufacturing âą Biotechnology
Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to prevent and treat serious bacterial infections. The company develops broad-spectrum conjugate and novel protein vaccinesâusing modern synthetic chemistry and a proprietary cell-free protein synthesis platform licensed from Sutro Biopharmaâto create difficult-to-make protein antigens more efficiently. Its lead programs are pneumococcal conjugate vaccine candidates VAX-31 (31-valent) and VAX-24 (24-valent) in Phase 2/3 studies, with earlier-stage candidates targeting Group A Strep and Shigella; Vaxcyte focuses on reducing invasive bacterial disease burden, antibiotic resistance consequences, and related morbidity in vulnerable populations.
âą Provide strategic and scientific leadership for process validation (PPQ, CPV, lifecycle validation) across commercial programs. âą Lead and facilitate execution of validation strategies to support technology transfer, site readiness, and product launch. âą Ensure alignment of validation activities with regulatory expectations and lifecycle management plans. âą Develop and implement risk management frameworks, tools, and processes in collaboration with Quality. âą Lead cross-functional risk assessments to identify, evaluate, and mitigate operational, technical, and regulatory risks. âą Monitor and communicate risk trends and key risk indicators to stakeholders. âą Support commercial manufacturing operations by ensuring processes remain in a validated and controlled state. âą Contribute to lifecycle management activities, including process improvements and continued process verification. âą Collaborate with Regulatory, CMC, Quality, Supply Chain, Procurement, and Engineering to support commercialization and supply continuity. âą Partner with internal teams and external CMOs to ensure alignment on validation and risk strategies. âą Provide guidance for validation of processes, systems, facilities, and methods within the commercial organization. âą Support deviation investigations, ensuring timely resolution and sustained compliance. âą Contribute to authoring and reviewing regulatory filings and responses to health authorities. âą Effectively communicate the scientific and commercial rationale for validation and risk management strategies. âą Provide leadership for execution of process validation and comparability activities, ensuring data integrity and compliance. âą Provide guidance on raw material qualification strategies to ensure supply reliability. âą Support validation activities across internal and external manufacturing networks. âą Communicate process validation performance and risk insights to key stakeholders. âą Build strong working relationships and influence across a matrixed organization. âą Contribute as a key member of the Global MSAT organization to enable successful commercialization.
âą Degree(s) in Chemical or Biochemical Engineering, Chemistry, Biochemistry, or related discipline with a minimum of 9+ years of relevant experience for Ph.D., 11+ years for M.S./M.A., or 14+ years for B.S./B.A. âą Strong experience in biologics/vaccine manufacturing, including: âą Process validation (PPQ/CPV) âą MSAT, technical operations, or late-stage development âą Technology transfer and commercialization âą Experience in quality risk management (ICH Q9) and regulatory expectations âą Demonstrated leadership in matrixed or cross-functional team environments âą Ability to apply deep technical knowledge to develop strategies and drive execution âą Strong problem-solving, organizational, and strategic planning skills âą Excellent communication and stakeholder engagement skills âą Ability to analyze data and align stakeholders with organizational strategy âą Innovative and entrepreneurial mindset to drive continuous improvement âą An entrepreneurial and creative approach to developing new, innovative ideas that will stretch the organization and push the boundaries within the industry.
âą The compensation package will be competitive and includes comprehensive benefits and an equity component.
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