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
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
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 Control
Novartis Italia, located in Ivrea, is seeking a QA Officer responsible for quality oversight in GMP activities. This role involves validating production sites, responsible for batch shipment releases, and maintaining quality documentation.The ideal candidate holds a scientific degree
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
Senior French Prompt Engineer – Clinical AI / LLM | Remote in EuropeWe are looking for a Senior French-speaking Prompt Engineer / Applied Research Scientist to contribute to the development of AI-powered clinical documentation systems.In this
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, you
Responsibilities Be the Deputy of QC Head in managing, coordinating and approving the execution of the analytical activities for batch release and in raw materials and packaging materials acceptance according to the specifications; Maintain, review and approve the
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,
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 AccountabilitiesBe
Band Level 3 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
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
Job Overview We are seeking a detail-oriented and operationally aware Billing Expert to support the delivery, accuracy, and continuous improvement of billing operations across our products and billing environment. This role isn’t directly within the Billing
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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
Offerta di lavoro - Salesforce Developer Junior/Mid Descrizione dell’offerta di lavoro Seltis Hub D&I: azienda operante nel settore della consulenza informatica. Cercasi un/a Salesforce Developer junior/mid da inserire nel team per la progettazione, sviluppo e manutenzione
Questa offerta proviene dal sito Jobmetoo Seltis Hub D&I ricerca, per azienda operante nel settore della consulenza informatica, un/a Salesforce Developer junior/mid da inserire nel team per la progettazione, sviluppo e manutenzione di soluzioni basate su
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
OverviewExperteer 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 quality
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