CQV Lead: GMP Facilities & Equipment

Allozymes; Windsor; Sur place; CAD 89 000 - 138 000; Plein temps

Résumé du poste

BIOVECTRA is seeking a CQV Supervisor to lead the Facilities, Utilities and Equipment CQV program, ensuring GMP systems are commissioned, qualified, and maintained in a validated state throughout their lifecycle.

You will provide technical leadership to the Engineering Technician team and collaborate across Engineering, Manufacturing, Maintenance, and Quality to support CQV planning, execution, and continuous improvement, while aligning with regulatory expectations.

Qualifications

• Bachelor's degree in Engineering, Biotechnology, Biological Sciences, Food Science, Chemistry, Pharmaceutical Sciences, Life Sciences, or related technical discipline.
• Minimum three (3) years of relevant experience in pharmaceutical manufacturing or GMP environments.
• Experience with commissioning, validation, and lifecycle activities is highly valued.
• Familiarity with GMP documentation and quality systems.

Responsabilités

• Lead Facilities, Utilities and Equipment CQV program and ensure systems remain validated.
• Develop and maintain CQV schedules and coordinate resources for manufacturing and projects.
• Create and approve CQV documentation including IQ/OQ protocols and deviation reports.
• Provide technical oversight for thermal validation and related systems.
• Support QA investigations, CAPAs, and risk assessments with CQV input.
• Mentor Engineering Technicians and drive continuous improvement of CQV processes.

Connaissances

CQV leadership

GMP knowledge

Regulatory compliance

Technical writing

Multidisciplinary teamwork

Formation

Engineering degree

Biotech background

Outils

Kneat

Description du poste

BIOVECTRA is seeking a CQV Supervisor to lead the Facilities, Utilities and Equipment CQV program, ensuring GMP systems are commissioned, qualified, and maintained in a validated state throughout their lifecycle.

You will provide technical leadership to the Engineering Technician team and collaborate across Engineering, Manufacturing, Maintenance, and Quality to support CQV planning, execution, and continuous improvement, while aligning with regulatory expectations.