Manufacturing Process Engineer

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.

• 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

• At least five years of mechanical manufacturing or process engineering experience
• Experience in production within a highly regulated environment
• 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.