Senior Process Engineer CQV Activities

Position: Senior Process Engineer for CQV Activities
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

• 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.