Job Description SummaryThe QC Supervisor supports the QC Head to ensure that Quality Control processes for materials acceptance, batches, quality control and QC equipment validation/qualification are executed and fully compliant to cGMPs regulation, corporate and national guidelines. Job
Job Description SummaryManage Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems. Job Description In this role you will be required to work
Novartis Farmacéutica in Ivrea, Piemonte, is seeking a QC Supervisor to support the QC Head in managing quality control operations. Responsibilities include overseeing analytical activities, ensuring compliance with regulations, and managing QC staff. The ideal candidate holds
Summary The QC Supervisor supports the QC Head to ensure that Quality Control processes for materials acceptance, batches, quality control and QC equipment validation/qualification are executed and fully compliant to cGMPs regulation, corporate and national guidelines. About The
Experteer Italy is looking for a Qualified Person who will oversee manufacturing processes and batch release to ensure compliance with regulatory requirements and our GMP quality system. You will play a key role in collaborating with Quality
Novartis Italia is looking for a QC Supervisor to support the QC Head in ensuring compliance with Quality Control processes. You will manage analytical activities, maintain compliance records, and ensure proper storage of materials. The ideal candidate
The QC Supervisor supports the QC Head to ensure that Quality Control processes for materials acceptance, batches, quality control and QC equipment validation/qualification are executed and fully compliant to cGMPs regulation, corporate and national guidelines. Major Accountabilities Be
Overview Experteer OverviewAs a Qualified Person, you will independently oversee manufacturing processes and batch release in line with regulatory requirements and our GMP quality system. You will collaborate with Quality Control, Production, and site leadership to ensure product
Experteer Overview In this Site Quality Head role, you shape and safeguard the quality strategy for a complex Ivrea manufacturing site. You partner with site and global leadership to ensure compliant operations, continuity, and innovative improvements.
Summary Independently supervise, without any interference of third persons, manufacturing processes and control testing of the site, related to the drug manufacturing license, operating as Qualified Person according to the local law (Article 52 of the Legislative Decree n. 219
Summary Manage Quality aspects and projects within area of responsibility. Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems. About The Role In this role you will be required to work
Experteer Overview In this QA Officer role, you oversee quality control across GMP activities at the site. You work in shifts to ensure continuous compliance, support batch release, and maintain GMP documentation. You collaborate with QA peers to
Location: Ivrea, Italy #onsite Role Purpose Support the pilot plant ramp up and operationalization process through the creation of a compliant manufacturing and QC‑related quality system which comprises master batch records, logbooks, forms, and procedures. Support qualification
The QA Officer guarantees the quality oversight over the entire working time of the facility for all the ongoing GMP activities. In this role you will be required to work in shifts, including night turns and
Independently supervise, without third‑party interference, manufacturing processes and control testing related to the drug manufacturing license, operating as Qualified Person in accordance with Article 52 of Legislative Decree n. 219 of 24 April 2006 (EU directive 2001/83/CE)
Location: Ivrea, Italy (Onsite) Role Purpose During the pilot plant ramp up and operationalization support line units efforts in developing compliant manufacturing and QC-related quality system, with particular focus on master batch records, logbooks, forms, procedures. Oversee
Band Level 3 Job Description Summary Manage Quality aspects and projects within area of responsibility. Ensures and supports overall GxP conformity and compliance with the Novartis Quality Management Systems. Job Description In this role you will
Location: Ivrea, Italy. Novartis is unable to offer relocation support: please only apply if this location is accessible. Step into a pivotal leadership role where quality, compliance, and patient safety come together. As Site Quality Head,
Summary The QA Officer guarantees the quality oversight over the entire working time of the facility for all the ongoing GMP activities. About The Role In this role you will be required to work in shifts,
Summary Independently supervise, without any interference of third persons, manufacturing processes and control testing of the site, related to the drug manufacturing license, operating as Qualified Person according to the local law (Article 52 of the Legislative