Vision systems project engineer

Experteer Italy; Monza; On-site; EUR 45,000 - 65,000; Full time

Job summary

Experteer Italy seeks a on-site Validation Engineer to drive the qualification of automatic inspection systems in a GMP-regulated pharma environment. You will own validation documents and define setup strategies, while developing inspection recipes for new and existing products.

The role requires collaboration with cross-functional teams, troubleshooting expertise, and strong English communication. Prior pharma validation experience and familiarity with Körber, Optrel, Innoscan, SEA Vision or

Qualifications

• Validation of automatic inspection systems and qualification strategies.
• Develop and optimize inspection recipes for new and existing products.
• Provide technical expertise and troubleshooting to support operations.
• Participate in project teams for regulatory submissions (NPI).
• Pharma validation experience is helpful.
• Experience with automated inspection systems (Körber, Optrel, Innoscan, SEA Vision or similar).
• Proficient in English (written and spoken).
• IT knowledge: Trackwise, Minitab and MS Office tools.

Responsibilities

• Issue validation-related documents for automatic inspection systems and define setup/qualification strategies.
• Develop and optimize inspection recipes for new and existing products.
• Provide technical expertise and troubleshooting to support operational activities.
• Participate in project teams to discuss technical aspects of new product introduction for regulatory submission.

Skills

Interpersonal skills

Proactivity

Teamwork

English proficiency

Education

Engineering degree or similar

Tools

Trackwise

Minitab

Microsoft Office

Job description

In this role you drive the validation and qualification of automatic inspection systems used for sterile injectable manufacturing, ensuring compliance with GMP, FDA, and EMA standards. You will own technical documentation and participate in new product introduction projects, collaborating with cross-functional teams to optimize inspection recipes and system setups. Your work supports regulatory submissions and continuous process improvements, contributing to reliable, compliant manufacturing. This position offers a hands‑on opportunity to shape automation strategies within a large, values‑driven organization.

• Issue validation-related documents for automatic inspection systems and define setup/qualification strategies
• Develop and optimize inspection recipes for new and existing products
• Provide technical expertise and troubleshooting to support operational activities
• Participate in project teams to discuss technical aspects of new product introduction for regulatory submission
• Degree in Engineering or similar scientific degrees or consolidated experience
• Previous pharma experience or validation experience is helpful
• Experience with automated inspection systems (Körber, Optrel, Innoscan, SEA Vision or similar) is helpful
• Proficient English (written and spoken)
• IT knowledge: Trackwise, Minitab and Microsoft Office tools
• Excellent interpersonal skills, proactivity, team-oriented