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
Novartis Farmacéutica is seeking a Qualified Person in Ivrea to supervise manufacturing processes and ensure compliance with local regulations. This role guarantees that each batch of medicines produced meets all legal and quality standards. The ideal candidate
IT58 (FCRS = IT058) Advanced Accelerator Applications Italy Srl is seeking a qualified professional to manage Quality aspects and projects in Ivrea, Italy. The role involves ensuring GxP conformity and compliance within the Novartis Quality Management
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
Experteer Italy is seeking a dedicated QA professional to support the pilot plant ramp-up and establish a compliant manufacturing and QC quality system. The role involves overseeing initial validation activities and coordinating the QA shopfloor team
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
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
Summary Manage Quality aspects and projects within area of responsibility. Ensures and supports overall Gx P conformity and Compliance with the Novartis Quality Management Systems. About The Role In this role you will be required to
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
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
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
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
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 DescriptionIn this role you will be required to work in shifts,
Job Description 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
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
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 be required to
Experteer Overview In this role you will support the pilot plant ramp-up and establish a compliant manufacturing and QC quality system. You will oversee initial validation activities and QC PQs while coordinating the QA shopfloor team
Summary Location: Ivrea, Italy (onsite) Role Purpose During the pilot plant ramp‑up and operationalization, support line unit efforts in developing compliant manufacturing and QC‑related quality systems, focusing on master batch records, logbooks, forms, and procedures. Oversee initial
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
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.