Gmqa-0, QA Intern

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7bjevj

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. We are seeking a motivated intern to join our Quality Operations Team in the area of GMP (Good Manufacturing Practices) compliance. This internship offers a unique opportunity to gain practical experience in the pharmaceutical industry while contributing to the optimization of our quality assurance processes. **Key Responsibilities**: - Support compliance verification activities for production and analytical documentation to ensure product and analytical data release.




- Conduct QA data integrity reviews on analytical activities.
- Assist in the management and optimization of GMP compliance processes at the site.
- Participate actively in the improvement processes of quality systems.
- Interact with various departments across the site to ensure alignment and compliance with quality standards.
- Support the team in reviewing and updating existing documentation, with a focus on accurate recording and monitoring of activities. **Requirements**: - Degree in Pharmaceutical Sciences or related fields.
- Interest in GMP regulations and quality processes.
- Strong organizational skills and attention to detail.
- Ability to work both independently and as part of a team, managing deadlines effectively. **What We Offer**: - A stimulating and innovative work environment.
- Opportunities for learning and professional development.
- The chance to actively contribute to significant projects in the field of GMP. **What we offer**: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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!

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7bjevj