Associate Director, Process Validation

🕒 June 25

🏄 California – Remote

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đŸ’” $174k - $203k / year

⏰ Full Time

🔮 Lead

👔 Director

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Logo of Vaxcyte

Vaxcyte

201 - 500 employees

Founded 2013

đŸ„ Healthcare

🏭 Manufacturing

🧬 Biotechnology

Healthcare ‱ Manufacturing ‱ 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 vaccines—using modern synthetic chemistry and a proprietary cell-free protein synthesis platform licensed from Sutro Biopharma—to 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.

📋 Description

‱ 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. ‱ 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. ‱ 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. ‱ 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. ‱ Provide guidance for validation of processes, systems, facilities, and methods within the commercial organization. ‱ Support deviation investigations, ensuring timely resolution and sustained compliance. ‱ 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. ‱ Provide leadership for execution of process validation and comparability activities, ensuring data integrity and compliance. ‱ Provide guidance on raw material qualification strategies to ensure supply reliability. ‱ Support validation activities across internal and external manufacturing networks. ‱ Communicate process validation performance and risk insights to key stakeholders. ‱ Build strong working relationships and influence across a matrixed organization. ‱ Contribute as a key member of the Global MSAT organization to enable successful commercialization.

🎯 Requirements

‱ 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. ‱ Strong experience in biologics/vaccine manufacturing, including: ‱ Process validation (PPQ/CPV) ‱ MSAT, technical operations, or late-stage development ‱ Technology transfer and commercialization ‱ Experience in quality risk management (ICH Q9) and regulatory expectations ‱ Demonstrated leadership in matrixed or cross-functional team environments ‱ Ability to apply deep technical knowledge to develop strategies and drive execution ‱ Strong problem-solving, organizational, and strategic planning skills ‱ Excellent communication and stakeholder engagement skills ‱ Ability to analyze data and align stakeholders with organizational strategy ‱ Innovative and entrepreneurial mindset to drive continuous improvement ‱ An entrepreneurial and creative approach to developing new, innovative ideas that will stretch the organization and push the boundaries within the industry.

đŸ–ïž Benefits

‱ The compensation package will be competitive and includes comprehensive benefits and an equity component.

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