Regulatory Affairs Associate

2 settimane fa

Milano, Italia Norgine A tempo pieno

**The Regulatory Affairs Associate is responsible for assisting the Regulatory Affairs team in our Italian affiliate. Sound interesting? Then read on**

Ultimately, at Norgine, we look for the following skills and experience in our Regulatory Affairs Associate;
- Some experience in the pharmaceutical industry
- An awareness of the drug development process
- Developing regulatory knowledge for medicinal products and medical devices
- Developing product knowledge
- Ability to pragmatically interpret GxP and Code of Practice or internal processes requirements relevant to her responsibilities
- Training in Applicable Codes and keep up to date with applicable case law (Knowledge and skills should be maintained by appropriate updates and training)
- Demonstrates a good ability to analyse data
- Focused on customer needs, follows up on commitments and requests
- Good interpersonal skills
- Good verbal and written communication skills
- Works cooperatively within a team
- Good ability with Microsoft Office (Word, Excel, PowerPoint)
- Ability to communicate clearly in English

**Norgine has a direct presence in 16 European countries, as well as Australia and New Zealand. We also have a strong global network of partnerships in non-Norgine markets. We are a flexible and fully integrated pharmaceutical business, with manufacturing (Hengoed, Wales and Dreux, France), third party supply networks and significant product development capabilities, in addition to our sales and marketing infrastructure. This enables us to acquire, develop and commercialise specialist and innovative products that make a real difference to the lives of patients around the world.

  • Regulatory Affairs Associate

    1 settimana fa

    Milano, Italia Sonnedix A tempo pieno

    To apply, please submit a CV and Covering Letter explaining how your experience matches the requirements of our position and how your personal motivators and values align to Sonnedix purpose.**Vacancy Name** - Regulatory Affairs Associate - Italy (Milan) **Location** - Milan **Location Country** - Italy **Profile** - The Role: The Regulatory Affairs...

  • Global Regulatory Affairs Specialist

    4 settimane fa

    Milano, Italia Jefferson Wells Italia A tempo pieno

    Direct message the job poster from Jefferson Wells Italia SCOPO DEL RUOLO: Responsible for supporting global regulatory submissions and maintaining compliance with regulatory requirements for pharmaceutical products across multiple regions aligned with global regulatory strategies, with particular reference to EU. This role involves preparing regulatory...

  • Global Regulatory Affairs Specialist

    2 settimane fa

    Milano, Italia Jefferson Wells Italia A tempo pieno

    Direct message the job poster from Jefferson Wells Italia SCOPO DEL RUOLO: Responsible for supporting global regulatory submissions and maintaining compliance with regulatory requirements for pharmaceutical products across multiple regions aligned with global regulatory strategies, with particular reference to EU. This role involves preparing regulatory...

  • Regulatory Affairs Specialist

    5 giorni fa

    Milano, Italia Pharma D&S A tempo pieno

    **Regulatory Affairs Consultant** Pharma D&S ricerca per la sede di Cassina de' Pecchi (MI) un/una Regulatory Affairs Consultant - Lifecycle Management, con almeno due anni di esperienza nel ruolo. La risorsa selezionata si occuperà di: - Gestione della sottomissione regolatoria e valutazione dei dati tecnici di tutte le procedure regolatorie -...

  • Regulatory Affairs Manager

    4 settimane fa

    milano, Italia Cpl Life Sciences A tempo pieno

    Managing Consultant - Regulatory Affairs & Quality @ Cpl Life Sciencesob Title: European Regulatory Affairs ManagerLocation: Milan, Italy - HybridRemuneration: Competitive salary and packageRegulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is...

  • Regulatory Affairs Specialist

    1 settimana fa

    Milano, Italia LHH A tempo pieno

    Realtà multinazionale leader nel settore energetico ricerca una risorsa da inserire in qualità di Regulatory Affairs Analyst/Specialist nel dipartimento Regulatory & Institutional Affairs. A diretto riporto del Regulatory & Institutional Affairs Director. La risorsa si occupa di monitorare e analizzare il contesto normativo, e soprattutto regolatorio, in...

  • Regulatory Affairs Specialist

    3 giorni fa

    Milano, Italia Page Personnel Italia A tempo pieno

    Si cerca una figura di Regulatory Affairs Specialist. Si occupa in particolare di: - Coordinare la redazione del design dossier e del design history file relativo ai dispositivi medici; - Assicurare la compliance regolatoria del prodotto in relazione al mercato di riferimento (principalmente USA-FDA ed Europa-MDR); - Seguire l'iter di approvazione del...

  • Stage Regulatory Affairs

    2 settimane fa

    Milano, Italia Opella A tempo pieno

    Opella, azienda multinazionale farmaceutica, sta ricercando, per la propria sede di Milano, una risorsa da inserire in stage nel dipartimento Regulatory Affairs della BU Consumer Healthcare. Stage - Regulatory Affairs Management Il/la Tirocinante sarà inserito/a all'interno del Dipartimento CHC Science Hub - Scientific Affairs e supporterà il Tutor di...

  • Regulatory Affairs Manager

    3 settimane fa

    milano, Italia Subbyx A tempo pieno

    Get AI-powered advice on this job and more exclusive features.Direct message the job poster from ScientaPartnering with CDMOs to strengthen their Commercial TeamsWe're currently partnering with a leading global consumer health business to find an experienced Global Regulatory Operations Medicine Manager to join their dynamic Regulatory Affairs team.This is...

  • Medical Device

    4 settimane fa

    milano, Italia Altro A tempo pieno

    Medical Device – Regulatory Affairs DirectorResponsibilitiesLine management of 10 Regulatory Line ManagersEstablish and implement regulatory strategies ensuring new and existing products comply with the latest global requirementsTrain the team on EMEA / FDA requirementsQualificationsMinimum 8 years in regulatory affairs in the medical device...