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