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 xysqume 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

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