Validation Specialist: Process

2 settimane fa


Ivrea, Italia Altro A tempo pieno

A leading pharmaceutical company located in Piemonte, Italy is seeking a Validation Expert responsible for managing validation activities to ensure compliance with global regulatory requirements. The ideal candidate should have a scientific degree and experience in a sterile GMP environment, along with fluency in Italian and English. This is an entry-level full-time position with opportunities for professional growth.#J-18808-Ljbffr



  • Ivrea, Italia Jobs for Humanity A tempo pieno

    A healthcare organization is seeking a Validation Expert in Ivrea, Italy. This full-time role involves managing process validation activities and ensuring compliance with cGMP requirements. The ideal candidate will hold a scientific degree and have prior experience in a sterile GMP environment, alongside fluency in Italian and English. Key responsibilities...


  • Ivrea, Italia Altro A tempo pieno

    A healthcare organization is seeking a Validation Expert in Ivrea, Italy. This full-time role involves managing process validation activities and ensuring compliance with cGMP requirements. The ideal candidate will hold a scientific degree and have prior experience in a sterile GMP environment, alongside fluency in Italian and English. Key responsibilities...


  • Ivrea, Italia Novartis Italia A tempo pieno

    A leading pharmaceutical company located in Piemonte, Italy is seeking a Validation Expert responsible for managing validation activities to ensure compliance with global regulatory requirements. The ideal candidate should have a scientific degree and experience in a sterile GMP environment, along with fluency in Italian and English. This is an entry-level...

  • Validation Expert

    5 giorni fa


    Ivrea, Italia Altro A tempo pieno

    Job Description SummaryThe Validation Expert is responsible for executing and managing process primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.Job DescriptionMajor accountabilities...

  • Validation Expert

    7 giorni fa


    Ivrea, Italia Novartis A tempo pieno

    Job Description Summary The Validation Expert is responsible for executing and managing process primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions. Job Description Major accountabilities :...

  • Validation Expert

    2 settimane fa


    Ivrea, Italia Altro A tempo pieno

    The Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.About The RoleSupport site validation planning by writing and...

  • Validation Expert

    2 settimane fa


    Ivrea, Italia Altro A tempo pieno

    The Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.About The RoleSupport site validation planning by writing and...

  • Validation Expert

    5 giorni fa


    Ivrea, Italia Altro A tempo pieno

    The Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.About The RoleSupport site validation planning by writing and...

  • Validation Expert

    2 settimane fa


    Ivrea, Italia Novartis Italia A tempo pieno

    The Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions. About The Role Support site validation planning by writing and...

  • Validation Expert

    2 settimane fa


    Ivrea, Piemonte, Italia Novartis A tempo pieno 40.000 € - 80.000 € all'ano

    SummaryThe Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and changemanagement activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.About the RoleMajor accountabilities:Support site validation...