Quality Engineering Portfolio Director

Direct quality engineering governance, lifecycle risk management, and continuous improvement for complex chemistry and biological products. The schedule is full-time, with occasional travel.

This Director leads portfolio-level quality oversight while building high-performing QS&T and quality engineering capabilities. The work connects product development, MS&T, Manufacturing, Engineering, QC, Regulatory, Operations, and Clients. You will strengthen prevention-focused quality culture, compliance sustainability, product reliability, and patient or user safety through technical influence.

Key Responsibilities:

• Develop quality engineering teams for client and regulatory requirements
• Govern risk management for new products, processes, and technologies
• Identify systemic compliance and product performance gaps
• Reduce Cost of Poor Quality through data-driven improvement
• Support inspections, audits, complaints, and regulatory discussions

Requirements:

• 10+ years in quality, process development, or manufacturing
• Demonstrated biologics, peptides, or complex chemistry experience
• Deep knowledge of validation, supplier quality, and statistical methods
• Understanding of international standards and inspection readiness
• Ability to lead through influence, governance, and technical expertise

Apply quality engineering, risk management, and regulatory expertise to improve long-term portfolio health at Agilent Technologies.

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