![]() ![]() Experience with data analysis, scientific tools and literature searches will be highly valued.Ideally you have finished your second year of studies. You are currently studying Chemical Engineering, Medicinal Chemistry, Biotechnology or similar.Various ad hoc assignments and general tasks.Preparation and follow-up activities for workshops and meetings.Supporting and assisting scientific consultants in their daily work.Tasks we will need your help with include: ![]() In this role, you will have the opportunity to develop your competencies and practical skills including preparing workshops and documenting the development. ![]() Peckish after lunch? We got your back with soft drinks, treats and fruit.įriday is something special, let's enjoy a beer together.Įasy access and treehugger friendly workplace.Are you passionate about Medical Device or Pharma development and have you finalized the first 2 years of your engineering/science degree? Would you like to gain relevant work experience whilst working alongside talented and passionate colleagues in a fun-loving culture with an international vibe? We are looking for a Student Assistant with a scientific mindset to assist our R&D consultants who support Danish Pharma and Medical Device companies with a broad range of tasks. Social gatherings and games hang out with your colleagues. Get your caffeine fix to get you started and keep you going. Morning person or night owl, this job is for you. This job comes with several perks and benefits We encourage all interested candidates, regardless of age, gender, sexual orientation, race, nationality, disability, religion, or ethnic affiliation to apply for the position.įor more information or questions please contact us at and benefits Experience working with medical device regulations,.Experience with ISO13485, Good Manufacturing Practice,.Creating and maintaining QMS records related to CAPA, change control, customer complaints and training.Establishing strategies to launch products into new markets, including communication with relevant authorities.Reviewing and revising QMS procedures to ensure that they are efficient and effective.Assisting the R&D team and the QA team in updating and reviewing the Technical Documentation during product development and maintenance.And, you take responsibility for your tasks. On the personality side, you are structured, you can work both in groups and on your own, and you enjoy learning new stuff. 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. You are interested in developing yourself to become a QA/RA professional or a project manager within health tech. You probably have a background in molecular biology, health technology or other related field, and you are in the final semester of a Bachelor's degree or have just started a Master's degree. Several development projects are in the pipeline, and we are also looking into expansion to new markets in near future. via a 510(k) process and was one of the first products to receive a CE marked as a class IIa device according to the European Medical Device Regulation. We are QMS certified according to ISO 13485 and our first product has been cleared for market in the U.S. Radiobotics is a multiple award-winning Danish health tech startup, developing software as a medical device for radiology, orthopedic and emergency departments and, aiding healthcare professionals in interpreting x-rays, with a focus on improving efficiency and diagnostic quality. 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 SaMD products revolutionizing Radiology through Machine Learning & AI. ![]()
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