• Bachelor degree in Analytical Chemistry, Pharmaceutical Sciences, or related field. 10+ years of experience in vaccine or biopharmaceutical industry with strong background in Quality Control or related analytical disciplines. Other combinations of education and/or experience may be considered.
• Proven success in matrixed environments with cross-functional coordination and strategic planning.
• Deep understanding of regulatory frameworks, data integrity, and method lifecycle requirements.
• Exceptional communication, negotiation, leadership and relationship-building
• Systems-thinking mindset and ability to identify leverage points in complex organizational structures.
• Experience with digital tools for data management, document review workflows, and collaborative project planning.
• Passion for mentoring, alignment building, and growing global technical communities
• Strong analytical and problem-solving abilities, with a focus on data-driven decision-making and continuous improvement.
• Level of Supervision: General Supervision
• The role will perform a variety of routine work within established policies and procedures. It is expected that the role receives rather high-level project information instead of detailed instructions on a weekly basis and general instructions on new projects and assignments.
• Reports to: Senior Director, Quality Control
• Reports to:
• Location: San Carlos, CA
• Location:
• Work Arrangement (may be adjusted based on business needs, job responsibilities, or changes to company policy):
• Work Arrangement