Location
burlington, halton region, Canada
Posted
July 16, 2026
Job Description
Advance your career as a CQV Engineer at IPS, where you will support commissioning, qualification, and validation in the life sciences industry. Join our expert team to drive compliance and efficiency across projects.
IPS is seeking an experienced CQV Engineer to contribute significantly to our mission of delivering innovative solutions in life sciences construction and management. This role involves writing critical C/Q/V documents and executing protocols in compliance with industry standards. You will engage in field activities and collaborate with teams to ensure projects meet pharmaceutical, biotech, and medical device requirements.
Key Responsibilities:
• Write Commissioning, Qualification, and Validation documents
• Perform on-site activities, including FATs and SATs
• Compile data and prepare reports for C/Q/V activities
• Assist in troubleshooting field execution issues
• Collaborate with teams for start-up and vendor test...
IPS is seeking an experienced CQV Engineer to contribute significantly to our mission of delivering innovative solutions in life sciences construction and management. This role involves writing critical C/Q/V documents and executing protocols in compliance with industry standards. You will engage in field activities and collaborate with teams to ensure projects meet pharmaceutical, biotech, and medical device requirements.
Key Responsibilities:
• Write Commissioning, Qualification, and Validation documents
• Perform on-site activities, including FATs and SATs
• Compile data and prepare reports for C/Q/V activities
• Assist in troubleshooting field execution issues
• Collaborate with teams for start-up and vendor test...