Quality Assurance Operations Intern

Work Your Magic with us!  

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your role

You will be integral to our Quality Operations Team, directly contributing to GMP compliance through meticulous documentation management. Your focus will be on optimizing our documentation processes to meet stringent regulatory standards. You will be responsible for creating master templates for crucial GMP documents, including operational procedures. A key aspect of your role involves data collection and analysis to establish improved compilation standards, directly impacting operational efficiency. Furthermore, you will support the team in the critical task of reviewing and updating existing documentation, ensuring accuracy in recording and monitoring our activities. This internship offers a hands-on experience in the pharmaceutical industry, allowing you to make tangible contributions to our GMP framework.

Who you are

• Degree in CTF or a related scientific field.
• Strong interest in Good Manufacturing Practices (GMP) regulations and quality assurance processes within the pharmaceutical sector.
• Good organizational skills and attention to details.
• Capability to work effectively both independently, taking ownership of your tasks, and collaboratively within a team to achieve common goals.
• Good time management.
• Eager to learn and develop professional skills within a stimulating and innovative work environment.
• Proficiency in Italian and English.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!