CQV Engineer - Life Sciences Validation & Compliance Italy

CAI; Emilia-Romagna; On-site; EUR 45,000 - 57,000; Full time

Job summary

CAI is seeking a CQV Engineer to join its Italy operations. The CQV Engineer develops documentation to support Commissioning, Qualifications and Validation for pharmaceutical facilities, utilities, and equipment, including field verification and summary reports at client sites.

Ideal candidates have 4–8 years of FDA-regulated CQV experience, strong English, and willingness to travel 100% within Italy and abroad.

Qualifications

• BS or MS in a relevant science or engineering field, or equivalent hands-on experience.
• Minimum 4-8 years’ experience in commissioning/qualification in FDA-regulated environments.
• Experience with facilities/equipment startup, FAT/SAT, IQ/OQ/PQ workflows preferred.

Responsibilities

• Develop CQV documentation to support commissioning, qualification, and validation.
• Write and execute protocols, perform field verifications, and prepare summary reports at client sites.

Skills

Attention to detail

Multi-tasking

Initiative

Project leadership

Problem-solving

Independent work

Travel willingness

Microsoft Word

Microsoft Excel

Education

BS or MS in science/engineering

Tools

Microsoft Word

Microsoft Excel

Job description

CAI is seeking a CQV Engineer to join its Italy operations. The CQV Engineer develops documentation to support Commissioning, Qualifications and Validation for pharmaceutical facilities, utilities, and equipment, including field verification and summary reports at client sites.

Ideal candidates have 4–8 years of FDA-regulated CQV experience, strong English, and willingness to travel 100% within Italy and abroad.