Care Specialist M/F

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8pgfvx

Zambon is a multinational pharmaceutical and chemical company that focuses on innovation and development with the aim to improve the quality of people’s health and patients’ lives. 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 the treatment of 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. Zambon SpA is looking for a CMC Senior Specialist that will ensure the technical support for management of product registration dossier and will write and review the Quality Part of the CTD with internal and external resources. Managing of the CROs/CMOs performing all the necessary process development,



manufacturing and analytical activities required for all drug substance and drug product development activities in support of new dossier submission for registration and product lifecycle in collaboration with the other internal stakeholders. Managing of the CMC regulatory strategy for the submission and during the review phase by the Health Authorities. Designing plans for the validation and registration of API and DP as required by cGMP, ICH (International Conference of Harmonization) and FDA regulations. Writing and/or reviewing Module 3 of eCTD in collaboration with consultants as required; Degree in Life Sciences/Health Related Sciences (CTF/Pharmacy). ~5+ years of experience in Regulatory Affairs/CMC preferably in Corporate Roles. ~ Excellent knowledge of written and spoken English. Full-time Other and Research Pharmaceutical Manufacturing #

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8pgfvx