Regulatory Affairs Consultant
4 mesi fa
**JSB Solutions**, società di servizi nel settore Life Science che offre consulenza, gestione di studi clinici e sviluppo software, con 3 sedi in Italia (Firenze, Parma e Milano) è alla ricerca di un
**Regulatory Affairs Consultant**:
- (JSB.SRF.23.070)_ da inserire all'interno della nostra divisione degli affari regolatori.
**un’esperienza in ruoli di Regulatory Affairs**
**di almeno 3 anni**, maturata in aziende farmaceutiche.
- regolatorio di filiale italia;
- attività di CMC writing;
- lifecycle management;
- attività di espansione geográfica.
**Requisiti richiesti dal ruolo**:
- conoscenza delle linee guida ICH, AIFA, EU e delle normative e direttive internazionali;
- conoscenza delle norme GMP;
- ottima conoscenza della lingua inglese (scritto e parlato);
- disponibilità a trasferte su esigenza specifica del cliente;
- elevate capacità comunicative con clienti esterni e interni.
**Sede di lavoro**: Parma.
**Modalità di lavoro**:formula mista Ufficio - Smart Working.
-
Regulatory Affairs Consultant
3 giorni fa
Parma, Emilia-Romagna, Italia Policonsulting A tempo pienoAre you a regulatory affairs expert looking for a challenging opportunity? Policonsulting is seeking a highly qualified Consultant in MDR & ISO 13845 to join our team.Job DescriptionAs a Consultant in MDR & ISO 13845, you will be responsible for providing consultation services to clients, analyzing Regulatory MDR processes, identifying areas for improvement,...
-
Global Regulatory Affairs Project Manager
5 giorni fa
Parma, Emilia-Romagna, Italia Chiesi A tempo pienoAbout UsChiesi is a leading international research-focused pharmaceutical and healthcare group with a rich history of over 85 years. Headquartered in Parma, Italy, the company operates in 31 countries with a strong presence of over 7,000 employees. Our mission is to improve people's quality of life by acting responsibly towards society and the environment....
-
Global Regulatory Affairs Senior Project Manager
7 giorni fa
Parma, Emilia-Romagna, Italia Chiesi Farmaceutici A tempo pienoJob Title: Global Regulatory Affairs Senior Project ManagerAbout the Role:We are seeking a highly skilled Global Regulatory Affairs Senior Project Manager to join our team at Chiesi Farmaceutici. As a key member of our Global Regulatory Affairs team, you will be responsible for ensuring the coordination and management of regulatory digital projects and...
-
Global Regulatory Affairs Specialist
1 settimana fa
Parma, Emilia-Romagna, Italia Chiesi Farmaceutici A tempo pienoJob SummaryWe are seeking a highly skilled Global Regulatory Lead to join our team at Chiesi Farmaceutici. As a key member of our Global Regulatory Affairs Team, you will be responsible for managing the Corporate RD Pipeline and providing regulatory guidance to the RD Global Core Team.Main Responsibilities:Contribute to company success by collaborating with...
-
Regulatory Affairs Senior Project Manager
3 settimane fa
Parma, Emilia-Romagna, Italia Chiesi Group A tempo pienoJob SummaryWe are seeking a highly skilled Regulatory Affairs Senior Project Manager to join our team at Chiesi Group. As a key member of our Global Regulatory Affairs team, you will be responsible for ensuring the coordination and management of regulatory digital projects and initiatives throughout their lifecycle.Main ResponsibilitiesDevelop and execute...
-
Global Regulatory Affairs Senior Project Manager
2 settimane fa
Parma, Emilia-Romagna, Italia Chiesi Group A tempo pienoJob SummaryWe are seeking a highly skilled Global Regulatory Affairs Senior Project Manager to join our team at Chiesi Group. As a key member of our Global Regulatory Affairs team, you will be responsible for ensuring the coordination and management of regulatory digital projects and initiatives throughout their lifecycle.Main ResponsibilitiesDevelop and...
-
Global Regulatory Affairs Senior Project Manager
2 settimane fa
Parma, Emilia-Romagna, Italia Chiesi Group A tempo pienoJob SummaryWe are seeking a highly skilled Global Regulatory Affairs Senior Project Manager to join our team at Chiesi Group. As a key member of our Global Regulatory Affairs team, you will be responsible for ensuring the coordination and management of regulatory digital projects and initiatives throughout their lifecycle.Main ResponsibilitiesDevelop and...
-
Global Regulatory Affairs Senior Project Manager
3 settimane fa
Parma, Emilia-Romagna, Italia Chiesi Group A tempo pienoJob Title: Global Regulatory Affairs Senior Project ManagerJob Summary:We are seeking a highly skilled Global Regulatory Affairs Senior Project Manager to join our team. As a key member of our Global Regulatory Affairs department, you will be responsible for ensuring the coordination and management of regulatory digital projects and initiatives throughout...
-
Global Regulatory Affairs Senior Project Manager
7 giorni fa
Parma, Emilia-Romagna, Italia Chiesi Group A tempo pienoJob SummaryWe are seeking a highly skilled Global Regulatory Affairs Senior Project Manager to join our team at Chiesi Group. As a key member of our Global Regulatory Affairs team, you will be responsible for ensuring the coordination and management of regulatory digital projects and initiatives throughout their lifecycle.Main ResponsibilitiesDevelop and...
-
Regulatory Affairs Medical Device
1 mese fa
Parma, Italia Adecco Italia A tempo pienoLa divisione specializzata Adecco LifeScience ricerca, per conto di un'importante azienda operante nel settore Medicale, un/una: REGULATORY AFFAIRS La realt in questione è un'azienda italiana con sede in provincia di Parma, leader nella progettazione, produzione e commercializzazione di prodotti per il settore dentale e medicale. Riportando al Regulatory...
-
Regulatory Affairs Medical Device
3 mesi fa
Parma, Italia Adecco Italia S.P.A. A tempo pienoLa divisione specializzata Adecco LifeScience ricerca, per conto di un'importante azienda operante nel settore Medicale, un/una:REGULATORY AFFAIRSLa realtà in questione è un'azienda italiana con sede in provincia di Parma, leader nella progettazione, produzione e commercializzazione di prodotti per il settore dentale e medicale.Riportando al Regulatory...
-
Regulatory Affairs Medical Device
3 mesi fa
Parma, Italia Adecco Italia A tempo pienoLa divisione specializzata Adecco LifeScience ricerca, per conto di un'importante azienda operante nel settore Medicale, un/una: REGULATORY AFFAIRS La realt in questione è un'azienda italiana con sede in provincia di Parma, leader nella progettazione, produzione e commercializzazione di prodotti per il settore dentale e medicale.Riportando al Regulatory...
-
Regulatory Affairs Medical Device
2 mesi fa
Parma, Italia Adecco Italia A tempo pienoLa divisione specializzata Adecco LifeScience ricerca, per conto di un'importante azienda operante nel settore Medicale, un/una:REGULATORY AFFAIRSLa realtà in questione è un'azienda italiana con sede in provincia di Parma, leader nella progettazione, produzione e commercializzazione di prodotti per il settore dentale e medicale.Riportando al Regulatory...
-
Regulatory Affairs Specialist
4 settimane fa
Parma, Emilia-Romagna, Italia IQVIA A tempo pienoJob Title: GRA RA EU and International SpecialistOur client, Chiesi Farmaceutici, a leading pharmaceutical company with over 80 years of experience, is seeking a skilled GRA RA EU and International Specialist to join their team. This exciting opportunity is part of their expansion efforts, and they have entrusted IQVIA with the recruitment...
-
Regulatory Affairs Specialist
2 settimane fa
Parma, Emilia-Romagna, Italia IQVIA A tempo pienoJob Title: GRA RA EU and International SpecialistOur client, Chiesi Farmaceutici, a leading pharmaceutical company, is seeking a highly skilled GRA RA EU and International Specialist to join their team. This exciting opportunity is part of their expansion plans, and they have entrusted IQVIA with the recruitment process.Responsibilities:Under the guidance of...
-
Global Regulatory Affairs Senior Project Manager
2 settimane fa
Parma, Italia Chiesi Farmaceutici A tempo pienoDate: 8 Oct 2024 Department: Global Regulatory Affairs Team: RD, 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 healthcare group with over 85 years' experience, operating in 31 countries with more than...
-
Global Regulatory Affairs Senior Project Manager
2 settimane fa
Parma, Italia Chiesi Farmaceutici A tempo pienoDate: 8 Oct 2024Department: Global Regulatory AffairsTeam: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITAbout us Based 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...
-
Specialist, Labelling
4 mesi fa
Parma, Italia Chiesi Farmaceutici S.P.A. A tempo pienoSpecialist, Labelling & Compliance Regulatory Affairs, Global Rare DiseasesDate: Jul 11, 2024Department: GRD Regulatory AffairsJob Type: Direct EmployeeTeam: R&D, Pharmacovigilance & Regulatory AffairsContract Type: PermanentLocation: Parma, ITPurposeTo contribute to and oversee GRDRA regulatory information and documentation managed in RIMS and eDMS, and to...
-
Global Regulatory Affairs Senior Project Manager
3 settimane fa
Parma, Italia Chiesi Group A tempo pienoWho we are looking forPurposeEnsure coordination and management of regulatory digital projects and initiatives during each phase (discovery, planning, execution, launch and maintenance) Ensure adequate execution of cross functional projects, participate on project team as expert in regulatory digital project managementMain ResponsibilitiesEnsure proper...
-
Specialist, Labelling
4 mesi fa
Parma, Italia Chiesi Farmaceutici S.P.A. A tempo pienoSpecialist, Labelling Compliance Regulatory Affairs, Global Rare DiseasesDate: Jul 11, 2024Department: GRD Regulatory AffairsJob Type: Direct EmployeeTeam: RD, Pharmacovigilance Regulatory AffairsContract Type: PermanentLocation: Parma, ITPurposeTo contribute to and oversee GRDRA regulatory information and documentation managed in RIMS and eDMS, and to...