Software Quality Assurance Specialist, Aarhus

Vitrolife & Igenomix Brasil, part of Vitrolife Group; Denmark; On-site; DKK 520,000 - 660,000; Full time

Job summary

Vitrolife Group is seeking a Software Quality Assurance Specialist in Aarhus to lead manual verification and validation of IVF-related software and stand-alone applications. You will derive test cases from requirements, document results, and ensure compliance across the lifecycle, working closely with developers, product owners and UX designers.

The role emphasizes collaboration, defect reporting, and potential automation opportunities.

Qualifications

• Experience in software quality assurance, including manual testing and defect tracking.
• Nice-to-have: experience with hardware integration in medical software.
• Interest in test automation and AI-assisted testing.

Responsibilities

• Perform manual verification and validation of medical device software and stand-alone software.
• Read requirements and derive test cases; document results clearly.
• Identify opportunities for test automation with the team and implement where appropriate.
• Ensure QA compliance across the software lifecycle and collaborate with cross-functional teams.
• Report defects and mentor others in QA best practices.

Education

Bachelor’s degree in Computer Science, Engineering, Life Sciences, or equivalent

Tools

Jira

Xray

TestComplete

Job description

Aarhus

Locations Aarhus

Software Quality Assurance Specialist, Aarhus

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.

About The Role

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.

Your impact

• 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.

What You Bring

• 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

Who You Are

• 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.

Success in this role means

• 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.

About Vitrolife Group

Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We are supporting our customers by improving their clinical practice and the outcome of the patient’s fertility treatment.

Currently, we are approximately 1,100 people worldwide, headquartered in Gothenburg, Sweden. Vitrolife Group’s products and services are available in more than 125 countries, through our own presence in more than 25 countries and a network of distributors. We are a sustainable market leader and aim to be the preferred partner to the IVF-clinics by providing superior products and services with the vision to enable people to fulfill the dream of having a healthy baby.

The Vitrolife AB (publ) share is listed on the Nasdaq Stockholm.

Contact Mette Frier Høst HR Manager Denmark – HR & Sustainability