Validation Specialist: Process
2 settimane fa
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
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Validation Expert — GMP Process
7 giorni fa
Ivrea, Italia Jobs for Humanity A tempo pienoA 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...
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Validation Expert — GMP Process
5 giorni fa
Ivrea, Italia Altro A tempo pienoA 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...
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Validation Specialist: Process
2 settimane fa
Ivrea, Italia Novartis Italia A tempo pienoA 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...
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Validation Expert
5 giorni fa
Ivrea, Italia Altro A tempo pienoJob 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...
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Validation Expert
7 giorni fa
Ivrea, Italia Novartis A tempo pienoJob 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 :...
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Validation Expert
2 settimane fa
Ivrea, Italia Altro A tempo pienoThe 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...
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Validation Expert
2 settimane fa
Ivrea, Italia Altro A tempo pienoThe 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...
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Validation Expert
5 giorni fa
Ivrea, Italia Altro A tempo pienoThe 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...
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Validation Expert
2 settimane fa
Ivrea, Italia Novartis Italia A tempo pienoThe 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...
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Validation Expert
2 settimane fa
Ivrea, Piemonte, Italia Novartis A tempo pieno 40.000 € - 80.000 € all'anoSummaryThe 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...