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
D-ploy is a leading IT and Engineering Solutions company with operations worldwide. Our mission is to deliver innovative and D-ploy is an IT and Engineering Solutions company with operations throughout the EMEA region including Switzerland, Germany,
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
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 on
Summary The QC Technician performs Quality control analysis on finished Product as well as in incoming materials according to cGMP r and SOPs, performs routine GxP Compliance/ Operational activities according to Novartis Quality Standards and makes analysis
Experteer Overview In this Site Quality Head role, you shape and safeguard the quality strategy for a complex Ivrea manufacturing site. You partner with site and global leadership to ensure compliant operations, continuity, and innovative improvements.
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,
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.
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
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
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 Legislative
Novartis Italia in Ivrea seeks a Qualified Person to oversee drug manufacturing processes, ensuring compliance with national laws and quality standards. Key responsibilities include certifying production batches, managing documentation for health authority compliance, and collaborating with Quality
In this role you provide onsite support for OT and automation systems to ensure reliable production, focusing on troubleshooting, incident resolution, patching, backups, and compliant change execution. You will work with Siemens environments to maintain and
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
Experteer Overview In this role you will support the ramp up and operationalization of a pilot plant by building and maintaining compliant manufacturing and QC quality systems. You will work to ensure adherence to the Novartis
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 2001/83/CE)
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
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
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
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