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Job description
Role
Executive Director, GxP Center of Excellence (CoE) at Bristol Myers Squibb, leading enterprise-wide GxP quality strategies across GCP, GLP, and GVP domains.
Responsibilities
develop and operationalize the GxP CoE strategy
embed proactive risk management
ensure inspection readiness
oversee global inspection and vendor quality oversight
drive digital transformation in quality systems
Lead quality integration for combination products, diagnostics, and digital health technologies, and provide GxP support for M&A activities
Champion a culture of quality by advancing governance, risk management, training, and continuous improvement initiatives
Collaborate with R&D, regulatory, and external stakeholders to ensure compliance and operational excellence
Qualifications
Bachelor’s in a scientific discipline; 15–20+ years in pharmaceutical/biotech industry with at least 10 years in GxP quality leadership, including regulatory inspection experience and global regulatory knowledge.
Preferred
experience in a global biopharma setting
familiarity with GxP systems (Veeva Vault, CTMS)
exposure to medical devices, diagnostics, or advanced modalities such as gene or cell therapies
Senior Leadership
Senior leadership role with strategic influence across R&D and quality functions.
Work Setup
hybrid; travel expectations not specified.
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Worksite address
madison, NJ, 07940, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.