Vacant job

Baxter was founded 90 years ago and has approximately 60,000 employees globally. We save and sustain lives through medical innovations that are now found in nearly every hospital, clinic, and home around the world.

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

The R&D Sustaining department in Luleå is responsible for developing and improving our current product portfolio. This involves driving various types of projects aimed at increasing customer satisfaction, enhancing product quality, optimizing product design, and strengthening our products' competitiveness. A significant part of our responsibility is to ensure compliance with legal requirements in the various markets where we operate. We currently have 23 people, divided into two teams, working agilely according to the Scrum model.

About the position

As a System/Validation & Verification Engineer, you will ensure that our products meet established requirements and that the product specifications align with user needs and intended use. Specifically, this means:

• Updating requirement and risk documentation for our products and identifying project impacts on these.

• Planning verification, validation, and actions to ensure we meet established requirements and mitigate gaps against requirements or risks.

• Reviewer and Subject Matter Expert (SME) for design updates.

• Risk assessments for production deviations, CAPA, post-market surveillance, etc.

• Reviewing and approving verification and validation reports.

The work is carried out in close collaboration with other functions.

You will work with medical devices such as lifting aids from Liko's product portfolio.

Your background

You are an engineer with a technical focus or equivalent experience and have 3–5 years of work experience, preferably within medical technology (MedTech) and product development, industry, or equivalent. You are accustomed to working in projects and have experience in risk management and working with product requirements or product information (BOM, quality issues, statistics, etc.). It is a great advantage if you enjoy both theoretical and planning work. You should also be independent and used to planning your own work.

Who you are

You are structured and enjoy managing and coordinating a lot of information. You take ownership of your tasks and you plan, prioritize, and drive your processes forward effectively while never compromising on quality. 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 a week is offered if the work allows and in consultation with your immediate supervisor.