Together, we can beat cancer.
At Varian, a Siemens Healthineers Company, we bring together the world’s best talent to realize our vision of a world without fear of cancer. Together, we work passionately to develop and deliver easy-to-use, efficient oncology solutions.
We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what’s possible, to improve people’s lives around the world. We embrace a culture of inclusivity in which the power and potential of every individual can be unleashed. We spark ideas that lead to positive impact and continued success.
If you want to be part of this important mission, we want to hear from you.
Role Overview:
In this role, you will be part of a multi-national team within a global R&D organization, and will work in close collaboration with other talented teams to deliver industry-leading solutions in cancer care.
You will be responsible for engaging stakeholders (e.g., Project Managers, Test Architects, and V&V Leads, etc.) to understand the verification deliverables, environments and tools required to support R&D activities.
You will coordinate the successful verification of products according to applicable medical device and health software regulations. Your test management skills will allow you to contribute in defining requirements, coordinating reviews with engineering experts, documenting processes, and communicating with stakeholders in a timely manner.

Key Responsibilities:

• Manage and coordinate device verification activities to ensure release deliverables and timely testing activities.
• Coordinate testing activities with program counterparts and cross-site testing teams.
• Define, and coordinate deployment of the test environments required to support R&D activities.
• Complete project documentation and design traceability reports required for release.
• Educate cross-functional teams about test environments and related practices to create customer equivalent ecosystems.
• Acquire and maintain adequate product and digital ecosystem knowledge for understanding product and testing needs.
• Provide coaching on product lifecycle processes and test strategies required to fulfil regulatory requirements.
• Participate in design input analysis, test planning analysis, and issues associated with testing in all parts of the system.
• Lead non-product validation, ensuring the completion of tool validation deliverables according to Quality System Regulations

Skills & Experience Required:

• Master’s degree in Biomedical Engineering, Computer science, software engineering or equivalent knowledge and skills.
• Experience leading software testing projects or corresponding skills.
• Experience in the field of test strategy and management, including test planning, design scoping, scheduling, and reporting.
• Good understanding of software delivery environments (e.g., Dev, SIT, QA, staging, etc.), and both physical and virtual infrastructures.
• Experience in project management and coordination, including agile methods
• Ability to communicate fluently in both spoken and written English.

What we can offer:

• Inspiring work atmosphere with supporting work community.
• Meaningful work with the medical domain.
• International and cross-cultural working environment.
• Newly opened modern office located in the downtown of Helsinki.

LI-OS1

Varian is required to comply with all local and applicable regulations that may be associated with vaccine requirements for certain roles.
Fighting cancer calls for big ideas.
We envision a world without fear of cancer. Achieving this vision takes dedication and commitment from all of us, every single day. That’s why we celebrate and value the distinctly beautiful and intersectional identities of each of our employees. We are a mirror of our patient-base, which allows us to innovate. Big ideas come from everywhere, and the best ideas are fostered by our unique individual experiences. At Varian, we encourage you to bring your whole self to work and believe your bold and authentic perspective will help to power more victories over cancer.

TogetherWeFight

About Us
Together, we can beat cancer.
Imagine a world without fear of cancer. We do, every day. Varian Medical Systems is the world’s leading manufacturer of medical devices and software for treating and managing cancer. For more than 70 years, we have developed, built, and delivered innovative cancer care technologies and solutions for our clinical partners around the globe to help them treat millions of patients each year.
Taking an Intelligent Cancer Care approach, we are harnessing advanced technologies like artificial intelligence, machine learning, and data analytics to advance cancer treatment and expand access to care to help patients become survivors.
When you join Varian, you become part of a global network of innovative and inspired minds working together across the globe. We keep the patient and our clinical partners at the center of our thinking as we power new victories in cancer care. Because for cancer patients everywhere, their fight is our fight.

• Manage and coordinate device verification activities to ensure release deliverables and timely testing activities.
• Coordinate testing activities with program counterparts and cross-site testing teams.
• Define, and coordinate deployment of the test environments required to support R&D activities.
• Complete project documentation and design traceability reports required for release.
• Educate cross-functional teams about test environments and related practices to create customer equivalent ecosystems.
• Acquire and maintain adequate product and digital ecosystem knowledge for understanding product and testing needs.
• Provide coaching on product lifecycle processes and test strategies required to fulfil regulatory requirements.
• Participate in design input analysis, test planning analysis, and issues associated with testing in all parts of the system.
• Lead non-product validation, ensuring the completion of tool validation deliverables according to Quality System Regulation