Product Quality Engineer – Medical Technology (m/f)

Are you passionate about quality in healthcare?

Excellent communicator – French and English – results-oriented, you are methodical, autonomous, persevering, and have an excellent team spirit and a very good sense of organization.

Generalist engineer, biomedical, mechanical or equivalent, you have initial experience in quality within the medical device, pharmaceutical or biotechnology industry (risk analysis, supplier quality management, production quality management, process validation). You have good knowledge of European (MDR) and American (FDA) regulatory requirements and experience in an ISO 13485 or ISO 9001 certified environment.

By joining Auctae as a product quality engineer – medical technology, you are the guarantor of regulatory compliance and the maintenance of the quality system. You master ISO 13485 and ISO 9001 standards, as well as common quality tools such as FMEA, CAPA, 8D, MSA, APQP, etc.

Your main tasks:

Are you Swiss or a national of one of the European Union member states?

Position open to all persons matching the profile. Permanent contract (CDI).

We are Auctae, a Swiss company based in the Lake Geneva region, driven by augmented innovation: engineering, project management, and the industry of the future.