- Preparazione documentazione regolatoria per AIC, variazioni e rinnovi;
- Gestione risposte alle deficiency letters;
- Registrazioni nazionali e decentrate;
- Traduzione e aggiornamento stampati;
- Redazione e aggiornamento dossier.
- Ottima conoscenza inglese o francese;
- Laurea in discipline tecniche/scientifiche;
- Specializzazione/master in regolatorio cosmetico;
- Conoscenza normative cosmetiche internazionali;
- Esperienza 1/2 anni in Regulatory Affairs cosmetiche;
- Ottima relazionalità e approccio interpersonale;
- Capacità problem solving;
- Attitudine al lavoro di squadra;
- Gestione stress.
-
Regulatory Affairs Resources Administrator
1 settimana fa
Chiesi Farmaceutici Parma, Italia**Date**: May 29, 2023 · **Department**: Global Regulatory Affairs · **Job Type**: Direct Employee · **Team**: R&D, Pharmacovigilance & Regulatory Affairs · **Contract Type**: Permanent · **Location**: · Parma, IT · About us · Based in Parma, Italy, Chiesi is an international res ...
-
Gra Eu Regulatory Affairs Junior Specialist
3 settimane fa
Chiesi Farmaceutici Parma, Italia**Date**: 30-Mar-2023 · **Department**: Global Regulatory Affairs · **Team**: R&D, Pharmacovigilance & Regulatory Affairs · **Job Type**: Direct Employee · **Contract Type**: Permanent · **Location**: · Parma, IT · About us · Based in Parma, Italy, Chiesi is an international rese ...
-
Govt., Pub. Aff.
2 settimane fa
Corteva Cremona, Italia**Description**:** Corteva Agriscience**, the world's first dedicated agriculture start-up, serves to enrich the lives of those who produce and those who consume, ensuring progress for generations to come. Our employees fulfill this purpose everyday by building/participating in a ...
-
Emea Regional Submission Partner
1 settimana fa
Corteva Provincia di Cremona, Lombardia, Italia**Description**:** GROWING WHAT MATTERS STARTS WITH YOU** · Corteva Agriscience, the world's first dedicated agriculture start-up, serves to enrich the lives of those who produce and those who consume, ensuring progress for generations to come. Our employees fulfill this purpose ...
-
Design Assurance Engineer
4 settimane fa
Fresenius Medical Care, Global Manufacturing, Quality & Supply Palazzo Pignano, Italia Permanent position, A tempo pienoGoal of function: · Assure the quality of design control activities and correctly realizing product development processes; · Maintenance of product compliance. · Main tasks: · Ensure that all design control deliverables comply with applicable regulatory requirements and des ...
-
GRA RA EU and International Specialist
3 settimane fa
IQVIA Parma, Italia A tempo pienoOur client, Chiesi Farmaceutici – one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry - in order to expand their staff, entrusted to IQVIA the recruitment of a GRA RA EU and Interna ...
-
Pharma Digital Compliance Specialist
2 settimane fa
532 GlaxoSmithKline Manufacturing SpA Parma, ItaliaWe create a place where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. · ...
-
Global Nutrition
1 settimana fa
Barilla Group Parma, ItaliaBarilla is looking for a Global Nutrition & Wellbeing Manager within the RD&Q Unit with Fixed Contract. She/he reports to Global Nutrition & Wellbeing Director. The position is based in Parma. · Job Purpose · The Global Nutrition & Wellbeing Manager is responsible for providing ...
-
Global Reg-CMC Sr. Specialist
3 giorni fa
Chiesi Parma, ItaliaAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years' experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To achieve its mission of improving people's quality of life by ...
-
Real World Evidence Study Manager
3 settimane fa
Chiesi Farmaceutici S.P.A. Parma, ItaliaSelect how often (in days) to receive an alert:Real World Evidence Study Manager - Temporary Date: 3 May 2024Department: Global Clinical DevelopmentTeam: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: TemporaryLocation: Parma, ITAbout usBased i ...
-
Global Reg-Cmc Sr. Specialist
1 giorno fa
Chiesi Parma, ItaliaAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years' experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To achieve its mission of improving people's quality of life by ...
-
Clinical Program Leader
4 settimane fa
Chiesi Vicofertile, ItaliaAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years' experience, operating in 30 countries with more than 6,000 employees (Chiesi Group). To achieve its mission of improving people's quality of life by ...
-
Pharmacovigilance Specialist
4 settimane fa
Chiesi Group Parma, ItaliaWho we are looking for · Main Responsibilities · will be responsible for conducting comprehensive reviews of adverse event reports for investigational and post-marketed products, ensuring compliance with regulatory guidelines and completeness of documentation. · Assist in devel ...
-
Clinical Project Manager
6 giorni fa
Chiesi Farmaceutici S.P.A. Parma, ItaliaSelect how often (in days) to receive an alert: · Team: R&D, Pharmacovigilance & Regulatory Affairs · Job Type: Direct Employee · Contract Type: Permanent · Location: Parma, IT · About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and h ...
-
Senior DP Analytical Scientist
4 settimane fa
Chiesi Vicofertile, ItaliaAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years' experience, operating in 30 countries with more than 6,000 employees (Chiesi Group). To achieve its mission of improving people's quality of life by ...
-
Clinical Project Manager
4 settimane fa
Chiesi Vicofertile, ItaliaAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years' experience, operating in 30 countries with more than 6,000 employees (Chiesi Group). To achieve its mission of improving people's quality of life by ...
-
Pharmacovigilance Specialist
4 settimane fa
Chiesi Vicofertile, ItaliaAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years' experience, operating in 30 countries with more than 6,000 employees (Chiesi Group). To achieve its mission of improving people's quality of life by ...
-
Global Ra Junior Specialist Extra Eu
3 settimane fa
Chiesi Farmaceutici Parma, Italia**Date**: Jun 26, 2023 · **Department**: Global Regulatory Affairs · **Job Type**: Direct Employee · **Team**: R&D, Pharmacovigilance & Regulatory Affairs · **Contract Type**: Permanent · **Location**: · Parma, IT · About us · Based in Parma, Italy, Chiesi is an international res ...
-
Area Clinical Operations Lead
4 settimane fa
Chiesi Vicofertile, ItaliaAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years' experience, operating in 30 countries with more than 6,000 employees (Chiesi Group). To achieve its mission of improving people's quality of life by ...
-
Global Reg-cmc Sr. Specialist
4 giorni fa
Chiesi Farmaceutici Parma, Italia**Date**: 13 Jun 2024 · **Department**: Global Regulatory Affairs · **Team**: R&D, Pharmacovigilance & Regulatory Affairs · **Job Type**: Direct Employee · **Contract Type**: Permanent · **Location**: · Parma, IT · About us · Based in Parma, Italy, Chiesi is an international rese ...
junior regulatory affair - Cremona, Italia - Emilav Bergamo | Agenzia per il Lavoro
Descrizione
Posizione
La ricerca è per un JUNIOR REGOLATORY AFFAIR CON PREGRESSA ESPERIENZA NEL SETTORE COSMETICO.
Il ruolo, all'interno del dipartimento Regolatorio, si occupa della gestione delle procedure per assicurare la conformità dei prodotti alle normative internazionali e delle attività per l'immissione sul mercato europeo ed extra-europeo.
Responsabilità principali:
Riporto gerarchico: Responsabile Regulatory Affairs
Requisiti
Requisiti richiesti:
Altre informazioni
Contratto tempo indeterminato. RAL discussa in sede di colloquio. Full time da lunedì a venerdì. Sede di lavoro a CREMA (CR).
Il presente annuncio è rivolto a tutte le età e nazionalità.
