Join a energetic 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. Key Responsibilities:

- Provide oversight on CQV documentation including risk assessments
- Translate process requirements into GMP-compliant strategies
- Identify critical quality attributes and process parameters




- Apply risk assessments for qualification and testing scope
- Review and approve CQV lifecycle documentation Requirements:
- 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
- Familiar with GMP regulations and ICH guidelines
- Excellent stakeholder management and communication skills Leverage your CQV expertise and compliance knowledge to drive successful project outcomes with our Client.

📌 Senior Process Engineer for CQV Activities (Lunenburg)
🏢 DPS Group Global
📍 Lunenburg