Join to apply for the Senior CQV Specialist role at AtkinsRéalis

Join to apply for the Senior CQV Specialist role at AtkinsRéalis

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Please note that this job posting aims to create a pool of candidates for future needs.
Your Role Within The Team

• Provides technical and project leadership with a comprehensive understanding of the pharmaceutical industry design/build/validation processes and how they relate to Canadian, EU, and US FDA cGMP regulation requirements.
• Develops/reviews technical documentation for clients in regulated industries including qualification and validation protocols and reports, criticality assessments, ...