CQV Process Engineer

QCS Staffing Ltd; München; On-site; EUR 70,000 - 95,000; Full time

Job summary

QCS Staffing Ltd in Munich, Germany, seeks a CQV Process Engineer for a 12-month contract in Life Sciences. You will support commissioning and qualification activities for pharmaceutical projects in a dynamic team.

The role requires extensive experience in Engineering or Commissioning, strong knowledge of GMP/safety, and involvement in FAT, pre-commissioning, and start-up activities for complex drug manufacturing projects.

Qualifications

• Extensive experience in Engineering or Commissioning and Qualification Management.
• Technical qualification at third level or equivalent in Engineering.
• Extensive knowledge and demonstrated experience managing Commissioning activities.
• Qualification for Pharmaceutical / Biotechnology projects preferred.
• Knowledge of safety, GMP and environmental regulatory requirements.

Responsibilities

• Lead test planning and strategies, including Single Test Approach and OneCQV FAT activities.

Skills

Test planning

Commissioning management

FAT testing

Pre-commissioning

Safety compliance

Education

Engineering degree or equivalent

Job description

CQV Process Engineer – Germany, Munich – Initial 12-Month Contract – Life Sciences

Our client is a global leader in pharmaceutical innovation, specializing in the development and manufacture of cutting-edge drugs. As they continue to grow, they’re seeking an experienced CQV Process Engineer to support their dynamic team and drive forward groundbreaking projects in Munich.

What you’ll deliver:

• Test planning and test strategies, including Single Test Approach and OneCQV (combined equipment and automation testing)Factory Acceptance Testing (FAT), including support and participation in supplier-site testing activitiesIntegrated Automation and Equipment Systems Pre-Commissioning / Commissioning activities, including safe startup activities aligned with applicable CQV safety requirements

What you’ll need:

• Extensive experience in Engineering or Commissioning and Qualification Management
• Technical qualification at third level or equivalent in Engineering.
• Extensive knowledge and demonstrated experience managing Commissioning activities
• Qualification for Pharmaceutical / Biotechnology projects preferred
• Knowledge of safety, GMP and environmental regulatory requirements.