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

• Develope appropriate measurement systems (Gages) for ongoing product inspection

• Plan and execute Test Method validation (TMV).

• Actively participate to Engineering Studies for process characterization: collect data and execute/conduct various analytical/statistical analysis and interpretation as part of process improvements and day-to-day support

• Collaborate to 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 presentation to internal and external stakeholders

Your profile:

• Minimum Bachelor Degree in technical matter (Biomedical/Mechanical/ Automation engineering)

• Minimum of 3 years of analogous working experience in a manufacturing enviroment ( 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 is preferred

• Fluent to communicate in Italian and English, German is considered as a plus

The role is based in Mezzovico and couldrequire occasional availability to work on the RARON site. Position will be limited to approx. 7 months.

If in line with the requirements and interested in the position we will be glad to evaluate your application.