V&V Engineer
Luleå, Sverige
Type of Employment Full-time
Job position Validation engineer
Work model On location
Application due date 13 August 2025
Are you the one?

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives-where your purpose accelerates our mission.

Verification & Validation Engineer

Baxter was founded 90 years ago and employs approximately 60,000 people globally. We save and sustain lives through medical innovations that today can be found in almost every hospital, clinic and home, worldwide.

At Baxter's site in Alvik, Luleå, about 130 people work to develop, improve and manufacture Liko's product portfolio of lifting aids. Together we create a place where we feel good, are successful and inspire each other to do good work. We are proud winners of the Swedish LEAN Award 2021.

The R&D Sustaining department, Luleå, is responsible for developing and improving our current product portfolio. This means driving through different types of projects with the goals of increasing customer satisfaction, raising product quality, optimizing product design and strengthening the competitiveness of our products. A major part of our responsibility is to ensure that we meet regulatory requirements in the different markets where we operate. We are currently 23 people, divided into two teams.

About the position

As a V&V Engineer, you will ensure that our products meet set requirements and that the specifications of the product are in line with the user's needs and intended uses. In concrete terms, this means:

  • Plan and follow up tests and validations and ensure that results and decisions are based on a statistical basis.
  • Responsible for test procedures, templates and scripts for verification and validation.
  • Review and approve verification and validation reports.
  • Depending on the role in the project, also creation of verification reports and support in verification/validation testing.

Your background

You are an engineer with a technical focus or equivalent experience and have a few years of work experience, preferably in industry or equivalent. You are used to working in projects and it is an advantage if you have experience of project work and/or improvement work. You should also be independent and used to planning your own work.

Who you are

You are careful and structured; you like order and orderliness! You take ownership of your tasks and you plan and drive your processes forward in an efficient way while never compromising on quality. Structure comes naturally to you and you have the ability to prioritize your tasks in an independent way. You thrive in a global environment and have no problem building relationships. You are a team player and are communicative in both speech and writing.

We offer you an opportunity to be challenged and to grow in a world-leading medical technology company. You will work at our facility in Alvik outside Luleå. Flexible work (from home) 1-2 days per week is offered if the work allows and in consultation with the nearest manager.