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.

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