CQV Engineer – Lead Validation & Commissioning (Italy)

CAI; Town of Italy (NY); Hybrid; USD 39,475 - 52,246; Full time

Job summary

CAI is looking for a CQV Engineer to join operations in Italy. The role involves supporting the documentation for Commissioning, Qualification, and Validation of pharmaceutical facilities.

Ideal candidates should have 4-8 years of experience in an FDA regulated environment, attention to detail, and skills in problem solving and working independently. The position offers a gross annual salary ranging from €34,000 to €45,000, based on experience.

Qualifications

• 4 – 8 years’ experience in commissioning and/or qualification in FDA regulated industry.
• Experience with facilities startup and troubleshooting.
• Familiarity with cGMP and biotech manufacturing processes.

Responsibilities

• Develop documentation for Commissioning, Qualification, and Validation.
• Manage C&Q documentation lifecycle from SLIA to OQ completion.
• Support onsite and offsite activities like FATs and SATs.

Skills

Attention to detail

Technical problem-solving

Independent work

Team building

Proficient in Microsoft Word and Excel

Communication skills in English

Education

BS or MS in a relevant science or engineering field

Job description

CAI is looking for a CQV Engineer to join operations in Italy. The role involves supporting the documentation for Commissioning, Qualification, and Validation of pharmaceutical facilities.

Ideal candidates should have 4-8 years of experience in an FDA regulated environment, attention to detail, and skills in problem solving and working independently. The position offers a gross annual salary ranging from €34,000 to €45,000, based on experience.