Join a dynamic 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 • Solid 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