Global CMC

2 giorni fa


LAquila, Italia Dompé A tempo pieno

A leading biopharmaceutical company in L'Aquila is seeking a Regulatory Affairs CMC & Site Regulatory Specialist. In this role, you will manage regulatory bodies, prepare CMC documentation, and ensure compliance with all regulations affecting site activities. The ideal candidate will hold a Bachelor's or Master's degree in relevant fields and have experience in a similar role within the Pharmaceutical sector. Fluency in Italian and English is required, along with familiarity with various regulatory systems and documentation processes.#J-18808-Ljbffr



  • L’Aquila, Italia Dompé A tempo pieno

    At Dompé Farmaceutici, we are not just a pharmaceutical company, we are an innovation-driven organization with over 130 years of experience, committed to advancing science and improving human health.About the Role:The Process Development Associate Director leads technology transfer projects from development to clinical manufacturing, ensuring compliance...


  • L’Aquila, Italia Dompé A tempo pieno

    At Dompé Farmaceutici, we are not just a pharmaceutical company, we are an innovation-driven organization with over 130 years of experience, committed to advancing science and improving human health.About the Role:The Process Development Associate Director leads technology transfer projects from development to clinical manufacturing, ensuring compliance...


  • L’Aquila, Italia Dompé A tempo pieno

    At Dompé Farmaceutici, we are not just a pharmaceutical company, we are an innovation-driven organization with over 130 years of experience, committed to advancing science and improving human health.About the Role:The Process Development Associate Director leads technology transfer projects from development to clinical manufacturing, ensuring compliance...


  • L’Aquila, Italia Dompé A tempo pieno

    At Dompé Farmaceutici, we are not just a pharmaceutical company, we are an innovation-driven organization with over 130 years of experience, committed to advancing science and improving human health.About the Role: The Process Development Associate Director leads technology transfer projects from development to clinical manufacturing, ensuring compliance...