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,
* Review and release Production Risk Management documentation
* Produce reports and presentations to internal and external stakeholders
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
* Knowledge of German is a plus
* Strong organization skills - Rigorous and disciplined
* 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. 7 months.
If in line with the requirements and interested in the position we will be glad to evaluate your application.
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