Support the implementation and certification of molex in the various quality systems that govern operations, such as iso 9001, iatf ts16949, iso 13485, vda, fda, as9100, and other standards. Assist with both internal and external audits, ensuring that, based on audit results, our quality systems are maintained and improved as necessary.
our team
you will work in close collaboration with manufacturing, engineering, planning, mechanical, and human resources departments to coordinate requirements and ensure alignment with applicable quality standards.
what you will do
* form interdisciplinary teams and act as a facilitator, primarily to address customer quality notifications (qns).
* apply company procedures for managing these notifications and maintain direct communication with the customer to ensure they receive all necessary information.
* create and keep up-to-date the documents used in the production area when there are changes to inspection plans, engineering revisions, serial numbers, or part numbers.
* generate internal deviations, verifying with engineering whenever a product does not meet specifications; conduct relevant tests and measurements; seek internal approvals, and subsequently release the material, ensuring proper function upon delivery to the customer.
who you are (basic requirements)
* bachelor’s degree in engineering or a related field, with relevant experience in a similar position.
* experience in medical, automotive, and/or commercial quality engineering.
* knowledge of iso / iatf 16949 and iso 13485.
* advanced proficiency in english (conversational).
what will put you ahead
* experience with sap.
* training in internal auditing.
* proficiency in interpreting engineering drawings.
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