Jobdescription Are you interested in working for a global company that empowers the brands that empower the world? We are looking for: Quality Engineer Your responsibilities will include: Support the team that is dedicated to New Product introduction: participate to Design transfer meetings and provide input to DFMEA Ensure CTQ cascade from Design input up to the inspection plan Develop appropriate measurement systems (Gages) for ongoing product inspection Plan and execute Test Method validation (TMV). Actively participate in Engineering Studies for process characterization: collect data and execute/conduct various analytical/statistical analyses and interpretation as part of process improvements and day-to-day support Collaborate with projects for process improvement and automation implementation Develop control plans consistent with product classification, potential defect types, defect frequency Review and release Production Risk Management documentation Produce reports and presentations to internal and external stakeholders Qualifikationen Your profile: Minimum Bachelor Degree in the technical matter (Biomedical/Mechanical/ Automation engineering) Minimum of 3 years of analogous working experience in a manufacturing environment ( Medical Device, pharmaceutical, automotive preferred) or an equivalent combination of education and experience Experience in a highly regulated environment (knowledge of standards such as ISO13485, CFR 21 part 820, MDR) Knowledge of Six Sigma techniques and/or inferential statistical techniques is required MS Office, Agile, and Windchill is a plus Fluent communication in Italian and English Your skills: Strong organization skills - Rigorous and disciplined Independent Positive Persistent & Resilient, Ability to overcome business & personal challenges Proactive Strong communication skills at multiple levels of the organization Creative: Ability to translate complex situations into simple solutions Plans, schedules and performs moderately complex engineering projects to evaluate, select, and adapt or modify standard manufacturing techniques, procedures, and criteria to increase the efficiency of plant operations Flexible Precise The role is based in Mezzovico. Position will be limited to approx. 6 months. If in line with the requirements and interested in the position we will be glad to evaluate your application.