Role PurposeThe Engineering Lead serves the Engineering organization for TRD RLT, responsible for establishing, maintaining and improving engineering processes with respect to buildings, equipment, utilities and energy. The Engineering Lead also provides engineering related tools and
Location: Ivrea, ItalyRole PurposeAct as Isotope Project Lead (IPL) by providing specialist knowledge and expertise as a Subject Matter Expert (SME) of radioisotope production and purification, focusing on assessing, developing, and optimizing new technologies that support
Location: Ivrea, Italy (Onsite)Role PurposeDuring 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 the
Summary Location: Ivrea, Italy #onsite Role Purpose Lead and serve the Engineering organization for TRD RLT, responsible for establishing, maintaining and improving engineering processes for buildings, equipment, utilities and energy. The Engineering Lead also manages engineering
Location: Ivrea, Italy #onsiteRole PurposeSupport 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 and
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 Location: Ivrea, Italy #onsite Role Purpose Act as Isotope Project Lead (IPL) by providing the specialist knowledge and expertise as Subject Matter Expert (SME) of radioisotope production and purification with particular focus on assessing, developing,
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
Summary The QC Technician performs Quality control analysis on finished product as well as on incoming materials according to cGMP rules and SOPs, performs routine GxP compliance/operational activities according to Novartis quality standards and makes analysis
SummaryLocation: Ivrea, Italy (onsite)Role PurposeDuring 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 validation activities
Global Senior Trial Delivery Manager - Sponsor Dedicated Milan, Italy | Full time | Home-based | R Global Trial Delivery Manager services provide for the global coordination of clinical trial management activities for internally managed and/or
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Date: 17 Mar 2026 Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, IT
Global Senior Trial Delivery Manager - Sponsor Dedicated Milan, Italy | Full time | Home-based | R Global Trial Delivery Manager services provide for the global coordination of clinical trial management activities for internally managed and/or
# Key Account Manager (m/f/x) – Nephrology/IronBewerbenlocations: EMEA, IT, Remote, CSL Vifortime type: Vollzeitposted on: Heute ausgeschriebenjob requisition id: R- To strengthen our Business Unit Nephrology/Iron in Italy, we are currently hiring a# Key Account Manager
Select how often (in days) to receive an alert: Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Date: 17 Mar 2026 Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, IT Purpose An accomplished clinical
Medical Science Liaison - Ophthalmology Territory: Italy Position Summary: As a field-based extension of our Client’s Medical Affairs team, the Medical Science Liaison (MSL) will support our Client’s investigational compound currently in Phase III clinical trial
In this role you will be required to work in rotating shifts, including night turns. Major Accountabilities Perform the analysis of batches following specific training; Perform routine maintenance and cleaning, periodic microbiological verification of pharmaceutical areas quality