Engineering Validation Specialist

Bausch & Lomb GmbH; Laval (administrative region); On-site; CAD 60,000 - 80,000; Full time

Job summary

A global diversified pharmaceutical company in Laval is seeking a Validation Specialist to prepare qualification documentation for various systems and utilities. The role involves coordinating calibration activities and managing compliance with regulatory standards, including GMP. The ideal candidate will have a Bachelor's degree in Science or Engineering with 5 to 10 years of validation experience, strong knowledge of HVAC and control systems, and fluency in French and English.

Qualifications

• 5 to 10 years of experience in validation.
• Knowledge of HVAC and control systems.
• Knowledge of Canadian standards.

Responsibilities

• Prepare qualification documentation (IQ/OQ) for equipment and utilities.
• Support the instrument calibration program and coordinate calibration tasks.
• Manage documentation related to calibration of utility equipment.

Skills

HVAC systems knowledge

Control systems knowledge

Purified water systems knowledge

GMP knowledge

Good communication in French and English

Education

Bachelor’s degree in Science or Engineering

Job description

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact.

Job Description

Job Title: Validation Specialist – Engineering
Reports to: Director of Engineering
Number of Direct Reports: 0

1. Position Purpose

The role of the Validation Specialist is to prepare qualification documentation (IQ/OQ) for equipment and utilities, document changes made to equipment and utilities, and maintain calibration records for measuring instruments used by the building mechanical systems department.

2. Key Responsibilities

EQUIPMENT AND UTILITY QUALIFICATION

Prepares the annual SVMP for their sector (Engineering)

Prepares qualification documentation for equipment and utility systems (HVAC, control systems (DDC), compressed air, purified water, etc.)

CALIBRATION / CERTIFICATION

Coordinates documentation related to calibration of utility equipment

Coordinates documentation related to calibration of measuring instruments used by the building mechanical systems team

Coordinates and oversees the work of external contractors during HEPA filter certification testing

Coordinates and oversees the work of external contractors during scale certification testing (manufacturing, packaging, warehouse, QA)

Supports the instrument calibration program and coordinates calibration tasks for equipment to ensure timelines are met

PROJECTS

Participates in the planning, organization, and execution of projects related to building mechanical equipment

Provides support during equipment start-up and operation

Ensures execution of all tasks under their responsibility for equipment qualification in compliance with GMP, HSE, and other equipment-specific regulatory standards

Ensures AutoCAD drawings are updated when new equipment is installed or when modifications are made to equipment and/or utility systems

3. Management Responsibility

Under the supervision of the Director of Engineering, the Validation Specialist performs qualification work for new equipment and utilities. The role supports calibration activities for utility equipment and is responsible for coordinating the work of certain contractors and ensuring compliance with applicable standards. This position has no direct supervisory responsibilities.

4. Key Professional Relationships

Internal Partners: Production, Engineering Projects, HSE, Quality, Purchasing

External Partners: Service providers, project-related contractors

5. Required Knowledge and Skills

a) Education

Bachelor’s degree in Science or Engineering, or equivalent relevant experience

b) Languages

French and English

c) Experience and Specific Knowledge

5 to 10 years of experience in validation

Knowledge of HVAC and control systems

Knowledge of purified water systems

Knowledge of Canadian standards

Knowledge of the pharmaceutical industry

Energy and fluids (air, water, etc.)

HSE

GMP (Good Manufacturing Practices)

We are an Equal Opportunity Employer. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.