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JOIN THE JOURNEY!
Brighter is expanding and looking for a dedicated Medical Software Specialist to join Quality and Regulatory Department to be a quality and regulatory ambassador in software development team and coordinate the world of software engineering and medical device regulatory and quality management.
Your future role
The purpose of this role is to act as a bridge and subject matter expert between the Quality and Regulatory department and Software development, to create an understanding of what is to be prioritized in the Software development.
You will in cooperation with the software department ensure efficient implementation of applicable quality and regulatory requirements throughout development and maintenance of Brighter’s medical device software to achieve and sustain compliance with Regulatory demands.
In this role you will work side by side with the software project managers and in cooperation with SW project manager participate in the preparation of the software-related design and development documentation.
The role includes, but is not limited to, the following tasks:
Your profile
To be successful in this role you need to be innovative and creative by nature, motivated by problem-solving tasks, and have a great ability to reflect on the ongoing work. You should have the ability to see a holistic picture to help prioritize the production of software in pace with the need established at the Quality and regulatory department.
You should also be self-sufficient and be able to push your work forward through the process. Great technical communication skills and the ability to write and speak to different audiences in an appropriate language are crucial for this role.
The following experience/knowledge is strongly meriting:
A suitable academic background is a master’s degree or equivalent in science or engineering, preferably in IT/software engineering. You have at least eight years of work experience within the field.
You are fluent in English, both written and oral. As Brighter is a truly international company you don´t need to speak Swedish for this position.
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. 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. Our organizational structure is based on a network organization, which means that each one of us is expected to lead and take decisions, and in that responsibility and ownership. 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. To be successful in this role you need to be able to work in a high-pressure regulated environment with the ability to adapt to changing priorities. You are a problem-solver and have a great ability to reflect on the ongoing work. You should have good project management and relationship skills. Further on it’s important that you have a strong business understanding and want to be a part of Brighter’s journey.
This position is based in Kista, Stockholm. We recommend that you submit your application as soon as possible as selection and interviews are held continually.
We welcome your application!
This recruitment is being handled by Ekaterina Leonova at Talentor Sweden, ekaterina.leonova@talentor.com
Nyckelord | Regulatory Documentation, Quality Assurance, medical software, Regulatory Compliance, Requirement analysis |
Branschkategori | Hälsa / Sjukvård |
Bransch | Annat |
Arbetsgivare | Brighter |
Arbetsplats | Kista |
Titel | Medical Software Specialist - Brighter AB |
Sektor | Privat |
Anställningsform | Tillsvidare |
Antal tjänster | 0 |
Ekaterina Leonova Ms ekaterina.leonova@talentor.com +46(0)701976549 |