Deviation Jobs In Ivrea - 28 Job Positions Available

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 #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

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

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

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

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

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

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 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

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

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 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

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

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

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

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