We have a current opportunity for a Quality Manager on a permanent basis. The position will be based in Kaufering. For further information about this position please apply.

Your responsibilities include the management and coordination of cross-departmental quality management projects
You also support and moderate the development of immediate measures, determination of the causes of errors, corrective and preventive measures and implementation of effectiveness tests
In this role, you will be responsible for the independent creation, monitoring and updating of QM documentation, including quality guidelines and procedural instructions
You plan and carry out internal audits independently and promote interdisciplinary cooperation between development, production and quality assurance to optimize processes
You proactively communicate our quality guidelines internally and conduct process training
You also interpret and implement current laws and standards in the company
you support in identifying optimization potentials and solving complex issues
In addition, you will support the implementation of computer system validations

This is what we want from you:

You have several years of professional experience with quality management systems and quality assurance, preferably in the medical device sector
Your application experience includes ISO 27001, ISO 13485, MDD and ideally also MDR
Auditor training is desirable and you have already gained practical experience with risk analysis, FMEA and other quality methods
communication in English is not a challenge for you and you are a real team player