QC Cleaning Analyst

In this role, you contribute to a GMP Quality Control lab focused on cleaning analytical methods and validation to guarantee sterile manufacturing equipment is ready for production. You will join the QC-Cleaning team in Monza, working in an international, fast-growing environment. You will support method development and analytical testing for cleaning verification, leveraging chromatography, TOC, and spectrophotometry. You’ll operate under GMP, SOPs, and guidelines to ensure compliant testing and data handling.

This position offers hands‑on learning in sterile injectable drug manufacturing and process support with cross‑functional collaboration.
Responsibilities and Duties   Support implementation of protocols, reports, and documents and manage them per GMP, SOPs, and guidelines
Perform analyses following team leader instructions, SOPs, and analytical procedures
Perform other duties and support activities as assigned while complying with safety training
Provide testing support for production of sterile injectable drugs
Learn to perform analyses effectively and in GMP compliance
Manage and dispose of samples and prepare chemical solutions
Qualifications   Previous experience in a GMP Quality Control lab
Ability to perform common chemical analysis with chromatography, TOC, and spectrophotometry (preferred)
Experience in sampling of manufacturing equipment (preferred)
English and Italian languages (professional knowledge)
Knowledge of main chemical techniques (HPLC, TOC, UV)
Excellent knowledge of Office Suite

#J-18808-Ljbffr