Join to apply for the Quality Management System Specialist role at Stevanato Group 1 week ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Job Description We are looking for a Quality Management System Specialist to join our quality department in Piombino Dese (PD). Stevanato Group is an Italian multinational manufacturing company that develops and produces drug containment solutions in glass and plastics. The main production process involves the processing of glass tubes by forming and subsequent cleaning and sterilization of containers using highly automated machinery. The ideal candidate will ensure the management system's compliance with applicable standards, guidelines, and regulations; maintain the relevant quality management system, processes, procedures, directives, and tools, monitoring that they continuously meet requirements. Key Accountabilities Implement and maintain an up-to-date management system ensuring compliance with regulations, directives, standards, and requirements. Conduct continuous analysis to monitor changes in national and international standards and regulations, collaborating with involved functions. Assess system efficiency, propose improvements, and keep the management system updated with relevant changes, working alongside other functions such as the internal auditing team. Participate in procedure standardization across international plants and functions to promote best quality practices and a unified SG quality approach. Support audit and inspection preparations to demonstrate compliance of the quality management system. Identify compliance issues, evaluate risks, and implement corrective and preventive actions to reduce non-conformities. Participate in training processes to ensure compliance with standards and procedures, collaborating with HR and other relevant functions. Qualifications Master's degree in a scientific field. 3-4 years of experience in a similar role. Proficiency in Italian and English. Knowledge of regulatory requirements including cGMP, FDA regulations, and ISO standards. Knowledge of CAPA, Change, Deviations processes and techniques. Adherence to Stevanato Group’s Values : Trust and respect everyone; Be accountable; Be ethical, always; Listen and communicate with transparency and honesty; Deliver results. About Us We are a dynamic organization with valued employees and a culture of empowerment. We are growing and seeking talented, passionate individuals to join our team! Additional Details Seniority level: Mid-Senior level Employment type: Full-time Job function: Quality Assurance Industries: Pharmaceutical Manufacturing Referrals can increase your chances of interviewing at Stevanato Group by 2x. Set Job Alerts Sign in to receive alerts for “Quality Management Specialist” roles. Castelfranco Veneto, Veneto, Italy - 2 weeks ago Related Role Trainee Program - Quality/Production Coordinator J-18808-Ljbffr