Join a team! We are a global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes. We develop, manufacture and market a range of products, primarily in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices, international pharmaceuticals. Our 7,000 employees share a common goal and values, propelling us to provide essential care to millions of people globally. We seek dedicated individuals who share our sense of urgency, unity, and excellence.
We are looking for a trustworthy and respectful individual who consistently does the right thing. Someone who is imaginative and proactive, with a keen eye for what is possible. A perceptive and adaptive person who is action oriented. We need a disciplined, focused, and accountable team member. If you embody these values, come join our company and help us shape the future.
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 itwhere your skills and values drive our collective progress and impact.
English will follow

DESCRIPTION DE POSTE

Titre du poste : Contractuel, Validation - Ingénierie
Supérieur hiérarchique : Spécialiste, Validation - Ingénierie
Nombre de rapports directs : Zéro (0)

JOB DESCRIPTION

Job Title: Contractor, Validation – Engineering
Reports To: Specialist, Validation - Engineering

Number of Direct Reports: Zero (0)

• Main Job Functions

The role of the contractor in validation is to prepare the qualification documentation for:

• New equipment
• Existing equipment subject to modification
• Utility services (HVAC, compressed air, purified water, BMS, etc.)

The role also includes:

• Coordinating and executing the tests outlined in the protocols and coordinating any necessary corrections with other departments.
• Preparing and maintaining all documentation related to equipment qualification.
• Providing technical expertise for all aspects related to qualification.
• Management Responsibility

This position does not have any direct supervisory responsibilities.

• Key Professional Relationships (Internal/External)

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

External Partners: Service providers, contractors related to projects.

• Required Knowledge and Skills:
• Required Education

Bachelor’s degree in Science or Engineering

• Languages

French

English, an asset

• Experience and Specific Knowledge

5 years of experience in validation
Knowledge of Canadian and US standards

Familiarity with the pharmaceutical industry

• Specific Technical Skills Automation/Industrial ComputingEnergy and Fluids (air, water, etc.)HSEGxP (Good Manufacturing Practices)Regulation, equipment

Le masculin est utilisé dans cette publication sans préjudice, dans un souci de concision.
Bausch Health s’engage à respecter l’égalité des chances en matière d’emploi et se conforme aux lois sur l’égalité des chances en vigueur dans les endroits où elle exerce ses activités .
The masculine is used in this publication without prejudice for the sake of conciseness.
Bausch Health is committed to equal employment opportunity and complies with equal employment opportunity laws in effect wherever it operates.
Bausch Health is an EEO/AA employer M/F/D/V.

The role of the contractor in validation is to prepare the qualification documentation for:

• New equipment
• Existing equipment subject to modification
• Utility services (HVAC, compressed air, purified water, BMS, etc.

The role also includes:

• Coordinating and executing the tests outlined in the protocols and coordinating any necessary corrections with other departments.
• Preparing and maintaining all documentation related to equipment qualification.
• Providing technical expertise for all aspects related to qualification.
• Management Responsibilit

This position does not have any direct supervisory responsibilities.

• Key Professional Relationships (Internal/External