15 ott - Monza
Altro
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
#J-18808-Ljbffr
15 ott - Casier
Michael Page
15 ott - Milano
QuiCare
15 ott - Roma
Lvmh Group
15 ott - Chieti
VINCI Energies Italia