Junior Regulatory Affairs Intern

3 settimane fa


Parma, Italia Davines Italia Spa A tempo pieno

The Davines Group, founded in Parma in 1983, specializes in professional cosmetic products under the brands Davines for haircare and [ comfort zone ] for skincare.
Led by Chairman Davide Bollati and CEO Anthony Molet, the Group is headquartered in Parma at the Davines Group Village, alongside which stand the Scientific Garden and EROC - European Regenerative Organic Center - a research center focusing on regenerative organic agriculture stemming from a partnership with the Rodale Institute.
The Group became a B corp in 2016, and today has 8 offices, operates in 90 countries, and employs around 900 collaborators globally.
Since 2019, both the Italian and US subsidiaries have been Benefit Corporations.
JOB MISSION Ensure compliance with national and international regulations, through a complete and constant update and the implementation of the necessary compliance, in line with our sustainability principles.
DUTIES AND KEY RESPONSIBILITIES Approval of cosmetic product labels in accordance with the current regulations Check raw materials and formulas in accordance with the main markets of interest Preparation of documentation (formula, specifications, stability test...) Request certificates and legalizations Cosmetic product notifications in the EU, UK, Canada and California portals Documentation for extra-EU registrations PERSON SPECIFICATION AND REQUIREMENTS Accuracy, precision, cooperation, good understanding of regulatory texts, proactive Scientific background EQUAL EMPLOYMENT OPPORTUNITY In Davines Group we celebrate diversity, and inclusiveness is a crucial pillar of our Ethical Chart.
For this reason, Davines Group does not discriminate in employment on the basis of ethnics, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, age, parental status or other non-merit factor.
#J-18808-Ljbffr



  • Parma, Italia JSB SOLUTIONS S.R.L A tempo pieno

    **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...


  • Parma, Emilia-Romagna, Italia Policonsulting A tempo pieno

    Are 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,...


  • Parma, Emilia-Romagna, Italia Chiesi A tempo pieno

    About 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....


  • Parma, Emilia-Romagna, Italia Chiesi Farmaceutici A tempo pieno

    Job 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...


  • Parma, Emilia-Romagna, Italia Chiesi Farmaceutici A tempo pieno

    Job 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...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    Job 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...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    Job 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...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    Job 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...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    Job 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...


  • Parma, Emilia-Romagna, Italia Chiesi Group A tempo pieno

    Job 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...


  • Parma, Italia Adecco Italia A tempo pieno

    La 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...


  • Parma, Italia Adecco Italia S.P.A. A tempo pieno

    La 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...


  • Parma, Italia Adecco Italia A tempo pieno

    La 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...


  • Parma, Italia Adecco Italia A tempo pieno

    La 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...


  • Parma, Emilia-Romagna, Italia IQVIA A tempo pieno

    Job 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...


  • Parma, Emilia-Romagna, Italia IQVIA A tempo pieno

    Job 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...


  • Parma, Italia Chiesi Farmaceutici A tempo pieno

    Date: 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...


  • Parma, Italia Chiesi Farmaceutici A tempo pieno

    Date: 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...


  • Parma, Italia Chiesi Farmaceutici S.P.A. A tempo pieno

    Specialist, 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...


  • Parma, Italia Chiesi Group A tempo pieno

    Who 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...