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 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
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
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
Senior French Prompt Engineer – Clinical AI / LLM | Remote in Europe We are looking for a Senior French-speaking Prompt Engineer / Applied Research Scientist to contribute to the development of AI-powered clinical documentation systems
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
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
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
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
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