Lavori attuali relativi a Global Regulatory Affairs Specialist – Pharma - Bardi - Synergie Italia S.P.A.
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Regulatory Affairs Specialist
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Bardi, Italia Manpower A tempo pienoUn'agenzia per il lavoro cerca un Regulatory Affairs Specialist per un'azienda del settore chimico-farmaceutico. Il candidato deve appartenere alle Categorie Protette e avere una laurea scientifica. Le principali responsabilità includono la gestione della documentazione regolatoria e la collaborazione con i team per garantire la conformità normativa....
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Regulatory Affairs Specialist
30 minuti fa
Bardi, Italia Manpower A tempo pienoUn'agenzia per il lavoro cerca un Regulatory Affairs Specialist per un'azienda del settore chimico-farmaceutico. Il candidato deve appartenere alle Categorie Protette e avere una laurea scientifica. Le principali responsabilità includono la gestione della documentazione regolatoria e la collaborazione con i team per garantire la conformità normativa....
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Regulatory Affairs Specialist
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Bardi, Italia Openjobmetis S.P.A. A tempo pienoOverview Openjobmetis S.p.A., Agenzia per il Lavoro, ricerca per azienda cliente operante nella produzione chimico / cosmetico, 1 Regulatory Affairs Specialist. Nel settore cosmetico, il Regulatory Affairs garantisce che i prodotti siano conformi alle normative vigenti, gestendo la documentazione, valutando la sicurezza degli ingredienti e dei prodotti...
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Regulatory Affairs Specialist: Italy
1 giorno fa
Bardi, Italia Uriach Italy A tempo pienoRegulatory Affairs Specialist: Italy & RomaniaAssagoEUR 35.000 - giorni faA leading European nutraceutical company is seeking a Regulatory Affairs Specialist to join its team in Assago, Italy. The role involves ensuring product compliance with legislation, performing product registration activities, and supervising regulatory processes in Italy and Romania....
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Regulatory Affairs Specialist: Italy
1 giorno fa
bardi, Italia Uriach Italy A tempo pienoRegulatory Affairs Specialist: Italy & RomaniaAssagoEUR 35.000 - giorni faA leading European nutraceutical company is seeking a Regulatory Affairs Specialist to join its team in Assago, Italy. The role involves ensuring product compliance with legislation, performing product registration activities, and supervising regulatory processes in Italy and Romania....
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Regulatory Affairs Specialist: Italy
1 giorno fa
Bardi, Italia Uriach Italy A tempo pienoRegulatory Affairs Specialist: Italy & Romania Assago EUR 35.000 - 50.000 6 giorni fa A leading European nutraceutical company is seeking a Regulatory Affairs Specialist to join its team in Assago, Italy. The role involves ensuring product compliance with legislation, performing product registration activities, and supervising regulatory processes in Italy...
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Regulatory Affairs Specialist: Italy
13 minuti fa
Bardi, Italia Uriach Italy A tempo pienoRegulatory Affairs Specialist: Italy & Romania Assago EUR 35.000 - 50.000 6 giorni fa A leading European nutraceutical company is seeking a Regulatory Affairs Specialist to join its team in Assago, Italy. The role involves ensuring product compliance with legislation, performing product registration activities, and supervising regulatory processes in Italy...
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Regulatory Affairs Specialist
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Bardi, Italia Maw A tempo pienoMAW .agenzia per il lavoro, Filiale di Brescia Maw Filiale di Brescia è allla ricerca di 1 REGULATORY AFFAIRS SPECIALIST per azienda operante nel settore biomedicale sita a Brescia.La posizione: Ricerchiamo una figura da inserire nell'organico dell'ufficio regolatorio dedicato alla Product Compliance per la Business Unit dei dispositivi di Collection
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Senior Global Regulatory Affairs Specialist
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Bardi, Italia Serioplast A tempo pieno3 days ago Be among the first 25 applicantsSerioplast, a global leader in rigid plastic packaging, is looking for a Senior Regulatory Affairs Specialist to join our Quality team at our Global Headquarters in Seriate (BG).This is an exciting opportunity to be part of an international, dynamic, and results-driven environment where quality and continuous...
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Pharma Regulatory Affairs Specialist – Api
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Bardi, 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 – Pharma
5 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 eCTDManager 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-*****-Ljbffr
