CQV Program Lead - Facilities & Equipment

CA03 BioVectra Inc.; Windsor; On-site; CAD 89,000 - 138,000; Full time

Benefits offered by this job

Bonus

Stock options

Benefits

Job summary

Agilent Technologies Inc. in Windsor, Canada, is seeking a CQV Supervisor to lead the Facilities, Utilities and Equipment CQV program within our GMP environment.

You will guide engineering technicians, coordinate with multiple functions, and ensure systems remain validated throughout their lifecycle. The role emphasizes risk-based commissioning, qualification strategies, and lifecycle management for GMP facilities and equipment, with opportunities to drive continuous improvement and ensure

Qualifications

• Minimum three (3) years of relevant experience within pharmaceutical manufacturing or other GMP-regulated environments.
• Experience with commissioning and qualification, validation, or CQV lifecycle activities is an asset.
• Familiarity with GMP documentation and quality systems is preferred.

Responsibilities

• Lead Engineering's CQV program for facilities, utilities and equipment.
• Plan, coordinate and execute CQV activities across multiple projects and vendors.
• Support regulatory readiness and QA processes with CQV input and documentation.

Skills

CQV leadership

GMP knowledge

Technical writing

Cross-functional leadership

Education

Bachelor's degree in Engineering or related field

Tools

Microsoft Office

Kneat

Job description

Agilent Technologies Inc. in Windsor, Canada, is seeking a CQV Supervisor to lead the Facilities, Utilities and Equipment CQV program within our GMP environment.

You will guide engineering technicians, coordinate with multiple functions, and ensure systems remain validated throughout their lifecycle. The role emphasizes risk-based commissioning, qualification strategies, and lifecycle management for GMP facilities and equipment, with opportunities to drive continuous improvement and ensure