Support validation of automated and robotic medical-device assembly equipment in Cambridge, Ontario, with robust regulated-manufacturing and data-integrity knowledge.

This Senior Automation Validation Engineer validates equipment-based processes, computerized systems, and functional testing activities. You will address part traceability, electronic records, database transactions, system data flows, and regulated-industry controls. Medical-device assembly experience is strongly preferred, alongside protocol execution and automation architecture expertise.

Key Responsibilities:
Verify device assembly processes and equipment-based functional testing
Assess data-integrity controls against regulated-industry expectations
Confirm part traceability, records, transactions, and system data flows
Execute FAT, SAT, IQ, OQ,



and Test Method Validation
Collaborate with suppliers, quality, manufacturing, controls, and stakeholders

Requirements:
Six years working with industrial automation or assembly equipment
Experience in regulated manufacturing settings
Expertise authoring and executing validation protocols
Knowledge of databases, electronic records, traceability, and data integrity
Working knowledge of sensors, actuators, controls, vision, and robotics

Apply validation, traceability, data-integrity, and automation expertise to medical-device manufacturing systems onsite in Cambridge.

📌 Medical Device Automation Validation Engineer Cambridge (Canada)
🏢 United Pharma
📍 Canada