Maria Cristina Scalzitti

Biography

  GMP  in Teva Pharmaceuticals Good knowledge of Regulatory Guidelines, Good Manufacturing Practices (GMP), Data Integrity principles and analytical equipment of a quality control laboratory. Excellent ability to work in teams, especially good listening skills, dynamism, security, accuracy, versatility, ability to develop interpersonal relationships. Good ability to organize own work, setting priorities and taking responsibility. Reliable, quick to learn and with the flexibility to adapt to evolving situations and priorities. Proficient in standard operating systems and Office packages. Reporting to the Regulatory Affairs Manager Responsible for the following activities: Regulatory Support and Artwork Management 

Research Interest

Regulatory affairs, Pharmaceutical research