Quality Operations Intern
Pubblicato il 04-10-2026 - Zambon in Milano
Zambon is a multinational pharmaceutical and chemical company focused on innovation and development to improve people’s health and patients’ lives. Based on a valuable heritage but strongly focused on the future, its Vision is “Innovating cure and care to make patients’ lives better”. Zambon operates in the pharmaceutical and chemical business and is present in 20 countries with subsidiaries in three different Continents – Europe, America, and Asia – and over 2900 employees, with manufacturing units in Italy, Switzerland, France, China, and Brazil.
Zambon products are commercialized in 84 countries. The company is working on treating specialties and rare diseases, such as Parkinson’s disease and Cystic Fibrosis, and is well-established in 3 therapeutic areas: respiratory, pain, and women’s care.
The Role:
Support the quality oversight of external manufacturing activities, ensuring compliance, documentation management and coordination with contract manufacturers, affiliates and partners.
Main Responsibilities of the role:
- Review of batch release certificates and sharing with Affiliates/Partners.
- Management of the TrackWise system for deviations, changes and complaints including: registration of deviations, complaints and changes in the system for all contract manufacturers.
- Bi-weekly/monthly monitoring of TrackWise records for deviations, complaints and changes related to all contract manufacturers on the basis of the follow-up requests to contract manufacturers for these quality records.
- Sharing deviations, complaints, changes and master batch records with Partners/Affiliates in accordance with Quality Agreements in place.
- Support the management and the review of minor deviations, complaints and changes.
- Support the management and the review of master batch records impacted by minor changes.
- Support in the review of Product Quality Reviews (PQRs) and executed batch records of contract manufacturers.
- Monitor stability data received from contract manufacturers and support its evaluation.
What we are looking for:
- Degree in Pharmaceutical Chemistry and Technology (CTF), Pharmacy, Biotechnology, or related scientific disciplines.
- Good knowledge of Microsoft Excel and MS Office applications.
- Fluent in English, both written and spoken.
- Strong attention to detail, with a high level of accuracy, patience, and a meticulous approach to quality documentation and data review.
- Ability to work in cross functional teams and international environments