At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby.
As a Software Quality Assurance Specialist at Vitrolife, you will play a key role in ensuring the quality and reliability of our IVF-related software products, which integrate closely with advanced hardware. You will take ownership of manual verification and validation activities, working hands-on with complex systems to confirm compliance with both product requirements and regulatory standards. Through collaboration with cross-functional teams, you will identify issues early, produce clear documentation, and contribute to continuous process improvements. This is an opportunity to make a tangible impact on the safety and effectiveness of solutions that help people realize their dreams of becoming parents.
Perform manual verification and validation of software in medical devices and stand-alone software products for IVF-related applications.
Read, understand and derive test cases from requirements specifications.
Identify opportunities for test automation together with our software test automation engineer and develop automated tests when needed.
Ensure quality and compliance of complex medical device software across the entire lifecycle—starting with clear requirements, followed by thorough test planning, execution, and comprehensive documentation. Quality assurance is embedded from the very beginning, ensuring each phase supports regulatory and product standards.
Identify and report defects, working closely with developers, product owners, and UX designers.
Mentor and guide team members in best quality assurance practices.
Bachelor’s degree in Computer Science, Engineering, Life Sciences, or equivalent.
3+ years of software quality assurance experience, preferably with hardware integration; experience in medical/laboratory software is a plus.
Strong knowledge of manual testing, creating and executing test cases, and defect tracking.
Interest in test automation; experience with Gherkin or TestComplete is a bonus.
Interest in responsible application of AI solutions to automate parts of testing.
Familiarity with Jira test management tools (e.g. Xray).
Experience in regulated environments (such as medical or financial sectors) is an advantage.
Proficiency in English; Danish proficiency is a plus
Detail-oriented and organized, with a strong sense of responsibility.
Excellent communicator with the ability to document findings clearly and collaborate across teams.
Analytical mindset, capable of problem-solving and adapting to new situations.
Able to work both independently and as part of a diverse team.
Manual testing is executed thoroughly, and documentation is always clear, complete, and compliant.
There is a clear strategy on what needs to be tested manually and what should be automated.
Issues and risks are identified early and communicated effectively to relevant stakeholders.
Test processes and procedures are continuously improved.
You contribute positively to a collaborative and quality-focused team culture.
We review applications on an ongoing basis and will close the recruitment once we have found the right candidate. We look forward to receiving your application.
If you have any questions, please reach out to Recruiting Manager Maria Soler, msoler@vitrolife.com
The Vitrolife Group is a world-leading global provider of medical devices and genetic testing testing solutions. Dedicated to the reproductive-health market since 1994, we have grown by focusing on product development, groundbreaking research, consistent quality control and acquisitions of innovative companies in the industry.
In 2021, Vitrolife acquired Igenomix, a leader in reproductive genetic testing services primarily for IVF clinics. Together we are now the Vitrolife Group, a global leader in reproductive health focused on supporting our customers and patients worldwide to improve treatment outcomes – always with sustainability in mind. Based on science and advanced research capabilities, our aim is to deliver products and services for the entire reproductive-health journey, providing consistent performance and guaranteed quality.
Currently, we are approximately 1,100 people worldwide headquartered in Gothenburg, Sweden. Our products and services are available in more than 125 countries, through our own presence in more than 25 countries and a vast network of distributors for the rest of the world. We are on a mission to be the leading valued solution provider in reproductive health and to support customers with successful treatment outcomes.
