NOUS RECHERCHONS UN·E SPÉCIALISTE EN VALIDATION POUR REJOINDRE IQVIA LABORATORIES À LAVAL, CANADA.

Nous recrutons des innovateurs passionnés qui font progresser les soins de santé grâce à une collaboration réfléchie et inclusive. Si vous souhaitez découvrir une carrière porteuse de sens, rejoignez‑nous pour transformer et accélérer la recherche et le développement.

JOB SUMMARY:

You will be responsible for validating systems and equipment in a pharmaceutical lab environment, ensuring compliance with regulatory standards and quality requirements.

WHAT YOU’LL BE DOING:

• Author and execute validation protocols (IQ/OQ/PQ) for equipment and processes
• Ensure computerized system validation (CSV) in compliance with applicable standards
• Write technical validation reports and standard operating procedures (SOPs)
• Collaborate with cross-functional teams to ensure regulatory compliance
• Participate in validation project management

THE KNOWLEDGE, SKILLS AND ABILITIES NEEDED FOR THIS ROLE:

• Excellent technical writing skills
• Attention to detail, autonomy, and critical thinking
• Effective communication across international teams