QA Validation - Internship

Objectives of the internship:

• Familiarity with the flows that govern a chemical-pharmaceutical company;
• Familiarity with GMP regulations;
• Use of IT systems in use at the company (Trackwise, Priority, Smarteam, StarLIMS)

Activities::

• Management of GMP documentation including review (also in real-time), archiving and management of any anomalies collaborating with the involved department (mainly production and MS&T Validation);
• Surveillance on-site to evaluate activities in real-time related to validation (cleaning and process);
• Collaboration in writing documents for Annual Review regarding routine cleaning and validation activities;
• Support in managing deviations and related corrective/preventive actions, with data collection and analysis, as well as change management;
• Participation in coordination meetings between functions.