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 recent 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.

📌 Quality Engineering Portfolio Director (Charlottetown)
🏢 Allozymes
📍 Charlottetown