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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📌 Quality Engineering Portfolio Director (Prince Edward Island)
🏢 Allozymes
📍 Prince Edward Island