Novavax
Novavax is a global biotechnology company with a proven vaccine technology. We are focused on developing our R&D assets and establishing partnerships to leverage the value of our technology to help protect health. Our technology includes both our recombinant protein-based nanoparticle and Matrix-M™ adjuvant, which we use to accelerate the development of innovative vaccines against serious infectious diseases. We aim to maximize the impact of our cutting-edge technology and address areas of unmet need in global health.
r&d • business partnerships • nanoparticle protein-based technology • matrix-m • adjuvant
Senior Director - Clinical Quality Assurance
March 14
🦀 Maryland – Remote
💵 $171k - $230.8k / year
⏰ Full Time
🟠 Senior
🔧 QA Engineer (Quality Assurance)
🦅 H1B Visa Sponsor
Novavax
Novavax is a global biotechnology company with a proven vaccine technology. We are focused on developing our R&D assets and establishing partnerships to leverage the value of our technology to help protect health. Our technology includes both our recombinant protein-based nanoparticle and Matrix-M™ adjuvant, which we use to accelerate the development of innovative vaccines against serious infectious diseases. We aim to maximize the impact of our cutting-edge technology and address areas of unmet need in global health.
r&d • business partnerships • nanoparticle protein-based technology • matrix-m • adjuvant
📋 Description
• Provide leadership and collaborate with required functional areas • Ensure compliance with applicable Good Clinical Practices (GCP), Good Pharmacovigilance Practices (GVP) and Good Clinical Laboratory Practices (GCLP) • Build and maintain cross-functional relationships with key functional areas • Drive the design, analysis, and oversight of global clinical Quality Management System (QMS) policies and procedures • Manage and oversee the quality of GCP, GVP and GCLP activities. • Provide leadership, direction, and mentorship across all levels of the organization • Develop and administer budgets, plans, and performance requirements linked to the clinical quality assurance department. • Hire, develop, and retain clinical QA personnel. • Serve as primary contact in QA for the oversight of Clinical Studies • Collaborate with cross-functional management to drive clinical process improvements.
🎯 Requirements
• Bachelor's degree in a scientific discipline; Master's degree or higher preferred • 15+ years of experience in GMP pharmaceutical, biologics and/or vaccine manufacturing • 10+ years of leadership experience in GCP/GVP QA.
🏖️ Benefits
• Base salary • Annual bonus • Equity grants • Professional career development/growth opportunities • Medical • Dental • Vision • Rx • STD • LTD • Life • Optional Life • 401(k) plan
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