Senior Validation Specialist – GMP Processes

2 settimane fa


Ivrea, Italia Healthcare Businesswomen’s Association A tempo pieno

A leading healthcare organization in Ivrea, Italy, is looking for a Validation Expert to manage process, primary packaging, and cleaning validation activities. The ideal candidate should hold a scientific degree and have prior experience in a sterile GMP environment. The role involves writing and maintaining validation plans, reviewing protocols, and collaborating across functions to ensure compliance with regulatory standards. Fluency in Italian and English is required, alongside knowledge of quality management tools.#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 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...

  • Validation Expert

    4 giorni fa


    ivrea, Italia Novartis 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...


  • Ivrea, Italia Novartis Italia A tempo pieno

    A leading multinational pharmaceutical company in Ivrea seeks a Validation Expert responsible for executing compliance validation activities in a sterile GMP environment. The ideal candidate will manage process validation and collaborate for technical transfers with a focus on quality risk management. A scientific degree and experience in a similar role are...

  • Validation Expert

    2 settimane fa


    Ivrea, Italia Healthcare Businesswomen’s Association 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

    4 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 :...


  • Ivrea, Italia Novartis A tempo pieno

    A leading global pharmaceutical company in Italy is seeking a Validation Expert to manage primary packaging and cleaning validation activities to ensure compliance with regulatory requirements. The ideal candidate will have a scientific degree, experience in a sterile GMP environment, and be fluent in Italian and English. Key responsibilities include...

  • Validation Expert

    1 settimana fa


    ivrea, Italia Healthcare Businesswomen’s Association 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 accountabilitiesSupport...

  • Validation Expert

    3 settimane fa


    Ivrea, Italia Novartis Italia A tempo pieno

    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. About The Role Major accountabilities Support site...

  • Validation Expert

    1 settimana fa


    ivrea, Italia Jobs for Humanity A tempo pieno

    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.About the RoleMajor accountabilities :Support site validation...