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At SmartWise we are developing and manufacturing a first-in-class endovascular delivery device whichenables direct tissue/organ infusions to hard-to-reach organs and tumors. Due to the unique mechanical properties and design, in animal studies, multiple infusions could be performed in extravascular tissue after exit of the vascular system, opening the door for future research into precise cell and biologic therapy delivery and repurpose small molecules for greater and safe local effects.
We are now looking for a Regulatory and Quality Engineer to join our team.
This is a fantastic opportunity for you who have been working a couple of years in the medical device field and want to develop a careertogether with a small team of experienced colleagues.
Key responsibilities
Practical experience
Education
Personal qualifications
Previous hands-on experience in regulatory filings of medical devices; experience in go-to-market as well as post-market surveillance of medical devices; additional territory experience, e.g. Korea, Japan are a merit
Interested? Submit your application today! We will review applications on an ongoing basis and hope to fill the position as soon as possible.
SmartCella is a world-leading biotech company pioneering the future of targeted therapies by combining first-in-class delivery platforms with cutting-edge cell and gene therapies. The SmartCella group consist of SmartCella Holding AB, ProCella Therapeutics AB, SmartWise AB and SmartCella Solutions AB with a total of 69 employees from more than 20 nationalities.