Manufacturing Process Engineer contract in Ottawa, fully onsite, focused on process validation, GMP compliance, and production optimization within nuclear medicine.

Actalent seeks a Manufacturing Process Engineer supporting development, implementation, and improvement in a highly regulated environment. You will collaborate with Manufacturing, Quality, Regulatory, and Operations teams. The work supports safe, compliant, efficient, and production-ready processes for nuclear medicine technologies and healthcare solutions.

Key Responsibilities:

- Develop and continuously improve manufacturing processes and production workflows
- Lead process validation and continuous improvement initiatives
- Create drawings, BOMs, specifications, and detailed work instructions
- Perform PFMEA, risk assessments, and root cause investigations




- Support equipment installation, commissioning, qualification, and optimization

Requirements:

- At least five years of mechanical manufacturing or process engineering experience
- Experience in production within a highly regulated workplace
- Hands-on process validation planning, execution, documentation, and analysis
- Experience troubleshooting equipment, tooling, fixtures, and mechanical processes
- Understanding of quality systems, GMP, and regulatory compliance

Apply your process engineering, validation, and compliance expertise to support reliable nuclear medicine manufacturing in Ottawa with Actalent.

📌 Manufacturing Process Engineer Ottawa
🏢 Actalent
📍 Ottawa