About the role
Are you currently looking for a part-time job in Aarhus? And are you considering a career within Quality Assurance or Regulatory Affairs? Join the exciting growth journey at Radiobotics and develop your skills in ISO standards, regulations, market registrations and much more in the health tech ecosystem, supporting the QA/RA objectives for Software as a Medical Device (SaMD) products revolutionizing Radiology through Machine Learning & AI.
Who you are
You probably have a background in molecular biology, health technology or other related field, and you are aiming at completing your degree within the next 2-3 years.
You are interested in developing yourself to become a QA/RA professional or a project manager within health tech. You are curious to learn how to develop and maintain a Quality Management (QMS) system in a regulated industry, and how to place medical device products in new markets.
On the personality side, you are structured, you can work both in groups and on your own, and you enjoy learning new stuff. And, you take responsibility for your tasks.
Tasks
- Supporting the registration of products into new markets, including communication with relevant authorities
- Creating and maintaining QMS records related to CAPA, change control, customer complaints and training
- Reviewing and revising QMS procedures to ensure that they are efficient and effective
- Driving projects aimed at improving the efficiency of the quality and regulatory processes
Nice to have
- Familiarity with ISO13485, ISO 62304, ISO 82304 and/or Good Manufacturing Practice
- Experience working with medical device regulations
How to apply
Check out the job listing on The Hub.
For more information or questions please contact us at [email protected].
