Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Location/Division Specific Information:

Within the Ferentino site you will be employed in Production Dept. and in particular in the Technical Production group working on Serialization, Performance monitoring and Digitalization

How Will You Make an Impact?:

The resource is responsible for performing activities in serialization systems to ensure proper connectivity with customer serialization systems in compliance with pharmaceutical serialization regulations. Additionally, the resource is responsible for analyzing and optimizing production performance by collaborating with departments to improve production processes. Moreover you'll be involved in Production DIgitalization projects

• Perform, monitor and maintain serialization system configuration in collaboration with customers.
• Evaluate production performance by analyzing critical metrics and other monitoring tools and identify areas for improvement
• Support and suggest Production Digitalization activities/projects

REQUIREMENTS:

Education: Degree in Engineering, Pharmacy, CTF, or technical/informatics diplomas.

High School Diploma, Secondary Education, Advanced Certificate, or equivalent.

Experience: at least 3 years of previous experience in a similar role, preferably in the pharmaceutical sector.

Preferred Knowledge in managing production performance and analyzing production processes.

Preferred: Minimum of 2 years of work experience in a manufacturing, operations, production or lab setting or related field

Preferred: Experience in a cGMP environment

Required: Good knowledge of English, both written and spoken.

Knowledge, Skills, Abilities:

• Required: Good analytical and problem-solving skills.

  Required: Ability to work in a team and manage complex projects.

Physical Requirements / Work Environment

You will work in our offices in Ferentino site in direct contact with colleagues and also with people from other Dept.