QA Operations Intern
Confirmed on the employer's own hiring board on Nov 10, 2026. First seen by Alion on Nov 10, 2026. EMD Group scores A on the Alion truth index.
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
As a QA Operations Intern, you drive GMP compliance across our pharmaceutical site within the Quality Operations team. You review analytical batch records and manufacturing documentation to ensure the compliant release of commercial product batches and analytical laboratory data. You perform rigorous quality assurance data integrity audits across analytical testing activities, identifying anomalies and preventing procedural deviations. You drive continuous process improvements by assessing and integrating practical artificial intelligence tools into team workflows. In addition, you review qualification and validation protocols for site equipment and manufacturing processes, collaborating with cross-functional departments to uphold all regulatory standards and maintain inspection readiness.
Who You Are
- Degree in Pharmaceutical Sciences or related scientific discipline.
- Strong interest in GMP regulations and quality assurance systems.
- Familiarity with data integrity, qualification, and validation.
- Predisposition to leverage AI tools for workflow optimization.
- High attention to detail and strong analytical mindset.
- Proven ability to manage deadlines and prioritize daily tasks.
- Ability to work independently and in cross-functional teams.
Salary Package
- € 400 - € 800/mese
- Mensa/ticket restaurant
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!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!