Vacant job

We are looking for you who have an engineering degree or equivalent and at least five years of experience in quality assurance of products and processes. The role involves ensuring that development and manufacturing follow ISO 13485, GMP, and internal quality standards, while driving improvement work and risk management forward.

Experience with technical documentation is central, where traceability, accuracy, and completeness are maintained throughout the entire product lifecycle.

Competence in non-conformance management is required to investigate causes, conduct analyses, and ensure effective CAPA measures.

The role also includes review and assessment of internal processes and suppliers, as well as support during external audits to ensure the highest level of compliance.

You are fluent in both Swedish and English, both verbally and in writing.

As a consultant at QRIOS Life Science & Engineering, you will work with exciting assignments within MedTech and Pharma for both large and small players. Here you develop quickly and have the support of an experienced QRIOS team behind you. In Malmö, we are 20+ specialists in project management, quality, and mechanics, many with over ten years of experience. We believe in delivering top performance without compromising life outside of work. We call this Work‑Life‑Passion, a culture where both performance and well-being have a place.