23 set - Bresso
Zambon
ppbZambon /b 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. /p h3The Role: /h3 pSupport the quality oversight of external manufacturing activities, ensuring compliance, documentation management and coordination with contract manufacturers, affiliates and partners. /p h3Main Responsibilities of the role: /h3 ul liReview of batch release certificates and sharing with Affiliates/Partners. /li liManagement of the TrackWise system for deviations, changes and complaints including: registration of deviations, complaints and changes in the system for all contract manufacturers.
/li liBi-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. /li liSharing deviations, complaints, changes and master batch records with Partners/Affiliates in accordance with Quality Agreements in place. /li liSupport the management and the review of minor deviations, complaints and changes. /li liSupport the management and the review of master batch records impacted by minor changes. /li liSupport in the review of Product Quality Reviews (PQRs) and executed batch records of contract manufacturers. /li liMonitor stability data received from contract manufacturers and support its evaluation. /li /ul h3What we are looking for: /h3 ul liDegree in Pharmaceutical Chemistry and Technology (CTF), Pharmacy, Biotechnology, or related scientific disciplines. /li liGood knowledge of Microsoft Excel and MS Office applications. /li liFluent in English, both written and spoken. /li liStrong attention to detail, with a high level of accuracy, patience, and a meticulous approach to quality documentation and data review. /li liAbility to work in cross functional teams and international environments /li /ul /p #J-18808-Ljbffr
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