Vaxcyte is a clinical-stage vaccine innovation company dedicated to engineering high-fidelity vaccines aimed at protecting humankind from serious bacterial diseases. With a focus on eradicating or treating infections such as invasive pneumococcal disease, Group A Strep, periodontitis, and Shigella, Vaxcyte is committed to addressing the significant health consequences of these conditions. The company operates under four core values: rethinking convention, aiming high, leading with heart, and modeling excellence, which guide their collaborative and innovative approach to vaccine development. Vaxcyte is positioned for success in the biotechnology sector, emphasizing quality assurance and regulatory compliance in its operations.
Join Vaxcyte as a Sr. Regulatory Document Formatting Specialist to format and finalize documents for regulatory submissions.
The Clinical Data Manager oversees data management activities for clinical trials at Vaxcyte, ensuring high-quality deliverables in collaboration with internal teams.
The Director for Drug Substance Commercialization will lead the launch readiness and commercial supply of glycoconjugate drug substances.
Seeking a Senior CAPA Manager to ensure compliance and maintain high standards in clinical quality assurance.
Join Vaxcyte as a Senior Clinical Document Specialist to support the electronic Trial Master File team in a dynamic regulatory environment.
Lead the commercialization of polysaccharides for glycoconjugate vaccines at Vaxcyte.
Vaxcyte is looking for a Director of Clinical Medical Writing to lead the development of regulatory and clinical documents in a fast-paced environment.
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