Do you have a couple of years of relevant experience from working within the MedTech industry? Do you have a genuine interest in working with quality and medical devices? Brighter AB (publ.) is now looking to recruit a junior QA specialist. Join the journey!
This is a chance to work with experienced colleagues within the MedTech industry and a chance to develop their skills within QA and RA and at the same time be a part of a company with a strong culture where we team up and win together.
Brighter is a health-tech company from Sweden with a vision of a world where managing chronic diseases is no longer a struggle. We believe a data-centric approach is key to provide smarter care for chronic conditions. Our daily-care solutions facilitate the flow of real-life treatment data between chronic-disease patients, their loved ones and their care providers – improving quality of life, easing the burden on healthcare systems, and opening new opportunities for data-driven research. In 2019 the company won the Swecare Rising Stars Award. For more information visit [ Link removed ]
Apply today as selection is ongoing and will interview candidates continuously.
We look forward to receiving your application!
As QA specialist you will have a supportive role in ensuring efficient implementation of Brighter’s quality management system processes. You will have a broad scope of tasks related to quality and regulatory compliance and be involved in implementing initiatives to drive continuous improvement.
You will work to ensure efficient implementation of applicable quality and regulatory requirements (such as MDR, ISO 13485) throughout development and maintenance of Brighter’s medical devices to achieve and sustain compliance.
Brighter today consists of 55 people and you will be part of a global team based in Kista and you will report to the Head of QA/RA
YOUR COMPETENCIES & BACKGROUND
We believe that you have a university degree in science or engineering and a minimum of 1 years of documented experience working with medical devices controlled by ISO 13485 and of MDD/MDR. You have knowledge of the regulations for design of medical technology products and experience of practical application of the requirements of relevant medical device regulations and standards. Professional fluency in Swedish and English is required.
To succeed in this role, you have a genuine interest in MedTech, you are reliable, have a high sense of responsibility and strong interpersonal skills. As a person you are eager to learn new things and have the confidence to take on new challenges but at the same time you are able to ask for guidance when needed. You have a structured and organized way of working and can handle multiple tasks independently as well as manage priorities in order to meet project timelines. It is important that you have a can-do attitude and the ability to creatively solve problems and to go the extra mile in order to succeed.
Be a brighterian.
At Brighter we have a genuine interest in driving change, our mission is to improve the quality of life of millions of people's. That goes for our teams as well. Our values are Smart, Friendly and Reliable and that is the guiding star for our attitudes and behaviors. How we lead ourselves and work together sets our company culture, and we thrive on having a company culture where we team up and win together. For us it's important that you are a team player and want to contribute to improving the world and Brighter's future success!
POOLIA LIFE SCIENCE