Join a agile team as a Senior Process Engineer, supporting capital projects with technical oversight of Commissioning, Qualification, and Validation (CQV) activities in a regulated pharmaceutical environment. Our Client is looking for a qualified Senior Process Engineer to ensure compliance and maintain inspection readiness. You will utilize your expertise in GMP principles and risk-based methodologies to oversee CQV documentation and strategy.

This role emphasizes compliance with regulatory standards while supporting project delivery effectively. Provide oversight on CQV documentation including risk assessments

- Identify critical quality attributes and process parameters
- Apply risk assessments for qualification and testing scope
- Bachelor’s degree in Engineering (Chemical, Mechanical, Electrical)
- At least 5 years' experience in CQV in a pharmaceutical setting
- Strong knowledge of pharmaceutical manufacturing processes
- Leverage your CQV expertise and compliance knowledge to drive successful project outcomes with our Client.

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📌 Process Re-Engineering Senior Expert (Lunenburg)
🏢 DPS Group Global
📍 Lunenburg