Regulatory Affairs Specialist
18 ore fa
Join to apply for the Regulatory Affairs Specialist role at Zambon Zambon is a multinational pharmaceutical and chemical company focused on innovation with the aim of improving people’s health and patients’ lives. It operates in 20 countries with subsidiaries across three continents – Europe, America, Asia – and has over 2,900 employees, including manufacturing units in Italy, Switzerland, France, China, and Brazil. Zambon’s products are commercialized in 84 countries and the company works on rare diseases such as Parkinson’s disease and cystic fibrosis, being well‑established in respiratory, pain, and women’s care therapeutic areas. The Role: Zambon SpA is looking for a Regulatory Affairs Specialist who will support regulatory activities for pharmaceutical products (especially OTC medicines), medical devices, food supplements, and cosmetics, ensuring compliance with national and international regulations. Main Responsibilities of the role: Support obtaining and maintaining registration of Zambon new and existing products worldwide Support local marketing companies (affiliates and distributors) to ensure fast product registration and optimal product life‑cycle management Support manufacturing plants in maintaining regulatory compliance and plan future regulatory changes Liaise directly with Health Authorities Interact with other company functions for the preparation and update of Core Company Data Sheets What we are looking for: Academic background: Degree in Life Sciences/Health Related Sciences (CTF/Pharmacy) Professional experience (minimum period – type): 4–5 years in Regulatory Affairs, preferably in Corporate Roles Skills: English (advanced level, written and spoken); knowledge of European and national regulations (EMA, MDR, EFSA); knowledge of eCTD Manager and Veeva Vault RIMS Ability to work in a team and manage multiple projects simultaneously Place of Work: Bresso (MI) Seniority level Associate Employment type Full‑time Job function Science, Research, and Other Industries Pharmaceutical Manufacturing #J-18808-Ljbffr
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Regulatory Affairs Specialist
1 giorno fa
Bresso, Lombardia, Italia Zambon A tempo pienoZambonis 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. 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...
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Pharma Regulatory Affairs Specialist – API
6 giorni fa
Bresso, Italia Altro A tempo pienoUna azienda farmaceutica leader in Lombardia cerca un Regulatory Affairs Specialist per supportare la gestione della documentazione tecnica e regolatoria per APIs. Il candidato ideale ha almeno 1-2 anni di esperienza, una laurea in discipline scientifiche e conoscenze approfondite delle normative farmaceutiche. Offriamo un contratto a tempo...
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REGULATORY AFFAIRS SPECIALIST
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Senior CMC Regulatory Specialist | Global Pharma
3 settimane fa
Bresso, Italia Zambon A tempo pienoA multinational pharmaceutical company is seeking a CMC Senior Specialist in Bresso, Italy. The role involves managing regulatory submissions and ensuring compliance with cGMP and FDA standards. Candidates should have a degree in Life Sciences and over 5 years of Regulatory Affairs experience. Excellent English communication skills are essential. This...
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3 settimane fa
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CMC Senior Specialist
3 settimane fa
bresso, Italia Zambon A tempo pienoJoin to apply for the CMC Senior Specialist role at ZambonZambon 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. Based on a valuable heritage but strongly focused on the future, its Vision is “Innovating cure and care to make...
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Global Medical Advisor
2 settimane fa
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