production supervisor

thermofisher · Ferentino, Italy

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Lingue richieste
Inglese professionale
Annuncio in
Inglese
Sede di lavoro
Ferentino, Italy
Modalità di lavoro
In sede
Pubblicata il
30 ottobre 2026

In breve

Thermo Fisher Scientific is seeking a Formulation Manufacturing Supervisor to lead sterile production operations. The company develops scientific solutions that protect the environment, ensure food safety, and advance medical research, aiming to make the world healthier, cleaner and safer. In this role you will oversee daily manufacturing activities in a GMP‑controlled sterile environment, ensuring that production schedules, quality standards and safety requirements are met. You will manage a team of roughly 50 operators and technicians, coach them, and monitor key performance indicators such as safety, quality, delivery, overall equipment effectiveness and yield. The position also involves supporting investigations, deviations, CAPA and change controls, while working closely with Quality, Engineering, Maintenance and Supply Chain to keep operations efficient. The ideal candidate holds a bachelor's degree in Life Sciences, Pharmacy, Engineering or a related discipline and brings at least five years of experience in sterile pharmaceutical manufacturing. Prior experience supervising large production groups of 40‑60 people is required, as is a solid understanding of GMP, aseptic processing and sterile manufacturing practices. Demonstrated leadership, strong problem‑solving abilities and effective communication skills are essential, together with a good command of English. Thermo Fisher offers a standard Monday‑to‑Friday schedule in an office‑based setting, supporting a culture of continuous improvement and Lean initiatives. The role provides the opportunity to influence a sizable team, collaborate across functions and contribute to the delivery of high‑quality products that have a global impact. What the role asks for: - Bachelor's degree in Life Sciences, Pharmacy, Engineering or related field - 5+ years sterile pharmaceutical manufacturing experience - Experience managing 40–60 production employees - Strong knowledge of GMP regulations - Expertise in aseptic processing and sterile operations - Proven leadership and team‑development skills - Excellent problem‑solving abilities - Good command of English language

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