Employee qualification with a direct link to the medical device industry

Oliver Mess, Management Representative

As a supplier to the international medical device industry, regulatory requirements and quality standards are an integral part of our day-to-day business. To develop our employees in a targeted way, we have been working with regular services for many years.

The support ranges from training courses and workshops on EN ISO 13485, QMSR (FDA), equipment qualification, process validation and statistical methods through to supplier management and the training of internal auditors. The focus here is not on the mere transfer of knowledge, but on practical and regularly updated application in everyday company operations.

What makes the collaboration especially valuable: the training courses are based not only on standards and regulatory requirements, but are also supplemented by numerous real-world examples from medical device manufacturers. This gives our employees a better understanding of the background to their tasks and the expectations of our clients.

The result: sustainable competence building, a shared understanding of regulatory requirements, and employees who can reliably translate quality requirements into practice.