Who we are
Vitae Evidence based within walking distance of Oslo’s Innovation District is building an innovative, exciting, and groundbreaking new
Digital Health solution in the field of Personalized Medicine.Our aim is to empower patients with
cancer, autoimmune or neurodegenerative diseases to live longer and better lives by helping them and their
healthcare providers discover the most precise, effective, and evidence-based treatment options. The Medical
Device Software Solution is CE-marked, which is a testament to our focus on quality and compliance with all
European health, safety, cybersecurity, and performance legislation.
Your impact
Quality and safety are paramount in Healthcare. You will play a key role in ensuring our medical software delivers reliable functionality with accuracy and precision, thus supporting our ability to
provide a frictionless, high-quality digital experience to scientists, patients and their healthcare team.
At Vitae Evidence, we strive to use our software skills to make a real difference to people’s lives, at scale.
How we work
We work with clinicians, molecular scientists and data engineers to harmonize patient-specific data, map it to literature based and real-world scientific evidence. Our software helps create personalized
insights tailored to individual medical records to provide Clinical Decision Support. We empower and enable patients to be actively involved in decision making through our web application and APIs.
We have early and frequent releases, encouraging a tight feedback loop between developers, our testers,
and our users.
We strive for high test coverage to enable us to move quickly and refactor without fear.
We make use of continuous integration to enhance the developers’ life and increase developer experience.
What you will do
Utilizes tools and methodologies defined by the Quality Management System (QMS) to ensure that the software tests identify defects and comply with quality standard.
Team up with product designers, software developers and regulatory specialist to timely deliver the most intuitive and useful medical device software releases.
Enhance product quality through manual testing and test automation.
Be part of building a growing team and implementing best practices.
Your skills and Experience
We believe that you will thrive working with Vitae Evidence if you are driven by purpose and want to contribute to making a difference in people's lives.
We are looking for you who have hands on experience with:
Quality assurance engineering;
Testing systems such as Cypress, Zephyr, Cucumber;
We also value the following skills
Good understanding of software processes and troubleshooting.
Ability to make considered decisions and to communicate them effectively.
Planning and organization. Working Agile (Scrum), using JIRA.
Finding joy in the detective work of diligent manual testing.
Have the ability and motivation to document test plans, configurations, test results and risk evaluations.
Bonus points for:
Experience working within healthcare regulatory constraints.
ISO 27001 (Information Security), ISO 14971:2019 (Risk Management), Software Life-cycle (IEC 62304).
Experience mapping data flows, architectures, and user paths.
Knowledge of continuous integration and delivery tools, such as Jenkins.
Familiar with Evidence Based Medicine, Real-World Research, Clinical Decision Support and Shared
Decision-making Best Practices.
