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p>Are you interested in working for a global company that empowers the brands that empower the world?
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p>We are looking for:
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p>Quality Engineer
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p>Your responsibilities will include:
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Support the team that is dedicated to New Product introduction: participate to Design transfer meetings and provide input to DFMEAEnsure CTQ cascade from Design input up to the inspection planDevelop appropriate measurement systems (Gages) for ongoing product inspectionPlan 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 supportCollaborate with projects for process improvement and automation implementationDevelop control plans consistent with product classification, potential defect types,
defect frequencyReview and release Production Risk Management documentationProduce reports and presentations to internal and external stakeholders
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p>
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p>qualifications
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p>
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p>Your profile:
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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 experienceExperience 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 requiredMS Office, Agile, and Windchill is a plusFluent communication in Italian, and English Knowledge of German is a plus
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p>Your skills:
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Strong organization skills - Rigorous and disciplined IndependentPositivePersistent & Resilient, Ability to overcome business & personal challengesProactiveStrong communication skills at multiple levels of the organizationCreative: Ability to translate complex situations into simple solutionsPlans, 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 operationsFlexiblePrecise
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p>The role is based in Mezzovico. Position will be limited to approx. 7 months.
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p>If in line with the requirements and interested in the position we will be glad to evaluate your application.
