Job Description SummaryThe QA Officer guarantees the quality oversight over the entire working time of the facility for all the ongoing GMP activities. Job Description In this role you will be required to work in shifts,
Job Description SummaryThe 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
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
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 manufacturing lines initial
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.
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
OverviewExperteer 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 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,
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 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
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
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
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
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
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
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
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
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
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