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Skåne län, Malmö
Previous experience is desired
74 days left
to apply for the job
We are looking for you who have an engineering degree or equivalent as well as at least five years of relevant experience in the following areas:
Planning and execution of validation activities
Responsibility for validation of equipment, processes, methods, and systems in accordance with current regulations, such as ISO 13485, MDR, GMP, GAMP5, and the company's quality system
Development and execution of validation plans, including ensuring correct and complete documentation
Participation in internal and external audits
You are fluent in Swedish and English, both in speech and writing.
As a consultant at QRIOS Life Science & Engineering, you will work on exciting assignments within MedTech and Pharma for both large and small companies. Here you will 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 results without compromising on life outside of work. We call this Work‑Life‑Passion, a culture where both performance and well-being have a place.
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