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
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 #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
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
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
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
Summary Location: Ivrea, Italy #onsite Role Purpose Support the pilot plant ramp up and operationalization process through the creation compliant manufacturing and QC‑related quality system which comprises master batch records, logbooks, forms, procedures. Support qualification and validation
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 to