Full-Time

Associate Director

Process Analytics

Confirmed live in the last 24 hours

Vaxcyte

Vaxcyte

201-500 employees

Develops vaccines for bacterial infections

Biotechnology
Healthcare

Compensation Overview

$190k - $197kAnnually

+ Equity Component + Comprehensive Benefits

Senior

San Carlos, CA, USA

This position is hybrid.

Category
Computational Biology
Biology Lab & Research
Biology & Biotech
Required Skills
Data Analysis
Requirements
  • PhD in Chemistry/Biochemistry or similar, with 7+ years of industry experience; MS with 10+ years of industry experience; or BS with 15+ years of industry experience.
  • Extensive experience in analytical method development, validation, and implementation for biopharmaceutical processes.
  • Strong knowledge of analytical techniques such as HPLC and colorimetric assays.
  • Experience working with bioconjugates or with regulatory submissions is a plus.
  • Proven track record of leading and managing analytical projects in a biopharmaceutical or biotechnology setting.
  • Excellent judgment when assessing risk – strong understanding of when to expend resources to reduce risk and when the level of risk is acceptable to move forward.
  • Excellent problem-solving skills and ability to work in a fast-paced, dynamic environment.
  • Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
  • Strong sense of organization, preferably with experience managing timelines using a tool such as Microsoft Project.
  • Strong ability to motivate, mentor, and connect with junior team members.
  • Curiosity and drive to quickly come up to speed; creativity to solve challenging problems.
Responsibilities
  • Serve as analytical SME for Conjugation department, representing the department in various cross-functional teams and meetings.
  • Review QC method validation protocols and reports to ensure that test method performance meets the needs of the process – if not, collaborate with QC team to bring performance up to process requirements.
  • Analyze manufacturing and stability data to identify trends in the process or analytical method performance.
  • Contribute to specification setting strategy using analysis of prior data and method performance.
  • Contribute to authoring and review of CMC sections in regulatory filings.
  • Contribute to analytical method development and optimization for new pipeline programs.
  • Coordinate characterization and in-process testing performed within the group.
  • Ensure analytical methods used for process development are fit for purpose.

Vaxcyte develops vaccines aimed at preventing bacterial infections, focusing on diseases like invasive pneumococcal disease, Group A Strep, periodontitis, and Shigella. Their lead product, VAX-24, is a pneumococcal conjugate vaccine that targets 24 strains of the Streptococcus pneumoniae bacteria and has received Breakthrough Therapy designation from the FDA for adult use. Vaxcyte employs advanced chemistry and a proprietary cell-free protein synthesis platform, XpressCF™, to create vaccines that can effectively address the complex defenses of bacteria while eliciting a strong immune response. Unlike traditional cell-based methods, their approach allows for the development of broad-spectrum vaccines. Vaxcyte's goal is to provide effective vaccines that can significantly reduce the impact of bacterial infections on global health.

Company Stage

IPO

Total Funding

$273.3M

Headquarters

Foster City, California

Founded

2013

Growth & Insights
Headcount

6 month growth

23%

1 year growth

61%

2 year growth

132%
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Simplify's Take

What believers are saying

  • Significant investments from major financial entities like Vanguard and Mutual of America Capital Management indicate strong market confidence in Vaxcyte's potential.
  • The recent $816.5 million raised through stock and warrant sales provides substantial capital for advancing their vaccine pipeline.
  • The appointment of experienced board members like John Furey can provide strategic guidance and enhance corporate governance.

What critics are saying

  • The success of Vaxcyte heavily depends on the clinical and commercial success of its lead product, VAX-24, which is still subject to regulatory approval.
  • The competitive landscape in vaccine development is intense, with numerous established players potentially overshadowing Vaxcyte's market entry.

What makes Vaxcyte unique

  • Vaxcyte leverages its proprietary XpressCF™ cell-free protein synthesis platform, which allows for more efficient and versatile vaccine production compared to traditional cell-based methods.
  • Their focus on broad-spectrum vaccines, such as VAX-24 targeting 24 strains of Streptococcus pneumoniae, sets them apart in the vaccine development landscape.
  • The FDA Breakthrough Therapy designation for VAX-24 underscores the innovative potential and clinical significance of their lead product.

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