Job Description SummarySupport GMP related activities—both operational and strategic—to ensure continuous compliance with applicable regulatory requirements, internal quality standards, and site procedures (SOPs). Actively contribute to the implementation, monitoring, and improvement of quality systems, providing expertise in GMP
Within the Quality Assurance team based in Saluggia, as Quality Engineer , you will support the development, manufacturing, release and post market surveillance activities associated with MicroPort CF products manufactured and released by the Saluggia plant. You will
Key Responsibilities Support GMP related activities—both operational and strategic—to ensure continuous compliance with applicable regulatory requirements, internal quality standards, and site procedures (SOPs). Actively contribute to the implementation, monitoring, and improvement of quality systems, providing expertise in GMP
Band Level 3 Job Description Summary Support GMP related activities—both operational and strategic—to ensure continuous compliance with applicable regulatory requirements, internal quality standards, and site procedures (SOPs). Actively contribute to the implementation, monitoring, and improvement of quality systems,
Summary Support GMP related activities—both operational and strategic—to ensure continuous compliance with applicable regulatory requirements, internal quality standards, and site procedures (SOPs). Actively contribute to the implementation, monitoring, and improvement of quality systems, providing expertise in GMP governance,
Novartis Farmacéutica in Saluggia is seeking a qualified professional to oversee GMP compliance in sterile production. The position requires a scientific degree and 2-3+ years of relevant experience. Responsibilities include supporting GMP activities, managing quality systems, and
Novartis Italia is seeking a qualified professional to support GMP compliance activities in Saluggia. The role involves driving improvements in manufacturing quality and ensuring adherence to internal and external quality standards. Ideal candidates should possess a scientific degree,
Job Scope The role oversees technical initiatives related to products already on the market and products undergoing registration in multiple countries. It ensures effective handling of testing and technical requests from Regulatory Authorities during registration, change,
Direct Category Specialist Published on: May 6, 2026 Job Category: Operations Employment type: Regular Full Time Obsessed by Science. Entrepreneurial by Nature. United by Purpose. Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions,
It ensures effective handling of testing and technical requests from Regulatory Authorities during registration, change, or renewal processes. Responsibilities include planning and executing IVD validation activities in alignment with company strategies, conducting scientific literature reviews, preparing