Regulatory Affairs Specialist
3 giorni 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
-
Global Regulatory Affairs Specialist
2 giorni fa
Bresso (MI), Italia Zambon A tempo pienoA multinational pharmaceutical company is seeking a Regulatory Affairs Specialist in Bresso, Italy. The role involves supporting regulatory activities for pharmaceutical products and ensuring compliance with national and international regulations. Ideal candidates will have a degree in Life Sciences, 4-5 years in Regulatory Affairs, and advanced English...
-
Regulatory Affairs Specialist
34 minuti fa
bresso, Italia Zambon A tempo pienoJoin to apply for the Regulatory Affairs Specialist role at ZambonZambon 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...
-
Regulatory Affairs Specialist
5 ore fa
Bresso, Italia Zambon A tempo pienoJoin 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...
-
Regulatory Affairs Specialist
4 ore fa
Bresso, Italia Zambon A tempo pienoJoin 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...
-
Bresso, Italia Zambon A tempo pienoA multinational pharmaceutical company is seeking a Regulatory Affairs Specialist in Bresso, Italy. The role involves supporting regulatory activities for pharmaceutical products and ensuring compliance with national and international regulations. Ideal candidates will have a degree in Life Sciences, 4-5 years in Regulatory Affairs, and advanced English...
-
bresso, Italia Zambon A tempo pienoA multinational pharmaceutical company is seeking a Regulatory Affairs Specialist in Bresso, Italy. The role involves supporting regulatory activities for pharmaceutical products and ensuring compliance with national and international regulations. Ideal candidates will have a degree in Life Sciences, 4-5 years in Regulatory Affairs, and advanced English...
-
bresso, Italia Synergie Italia S.p.a. 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...
-
REGULATORY AFFAIRS SPECIALIST
2 settimane fa
Bresso, Italia Synergie Italia S.p.a. A tempo pienoSynrgie Italia Spa, filiale di Monza, seleziona per azienda cliente produttrice di principi attivi farmaceutici, una figura di : REGULATORY AFFAIRS SPECIALIST In qualità di Regulatory Affairs Specialist, verrai inserita / o nel team dedicato agli Affari Regolatori e supporterai le attività legate alla gestione della documentazione tecnica e regolatoria...
-
REGULATORY AFFAIRS SPECIALIST
3 ore fa
Bresso, Italia Synergie Italia S.p.a. A tempo pienoSynrgie Italia Spa, filiale di Monza, seleziona per azienda cliente produttrice di principi attivi farmaceutici, una figura di : REGULATORY AFFAIRS SPECIALIST In qualità di Regulatory Affairs Specialist, verrai inserita / o nel team dedicato agli Affari Regolatori e supporterai le attività legate alla gestione della documentazione tecnica e regolatoria...
-
Global Regulatory Affairs Specialist
3 giorni fa
Turbigo (MI), Italia Alfasigma A tempo pienoA global healthcare company based in Italy is seeking a Non-Pharma Global Regulatory Affairs Specialist with at least 5 years of experience in regulatory affairs, especially in food supplements and medical devices. The role involves managing regulatory documentation for projects across EU and global markets, collaborating with various teams to ensure...
