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Salary
≈ $44k – $117k per year (Estimated)
Location
In office (Helsinki)
Seniority
Middle · 3+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 26, 2026. First seen by Alion on Oct 21, 2026. Elekta scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Elekta is a Swedish medical technology company headquartered in Stockholm that develops radiation therapy and radiosurgery systems, including the Elekta Unity MR-Linac, the Versa HD and Harmony linear accelerators, Leksell Gamma Knife Esprit and oncology software such as Elekta ONE. Founded in 1972 and listed on Nasdaq Stockholm, it employs more than 4,000 people with offices in over 40 countries, and its solutions treat more than 2 million patients a year in over 130 countries. Elekta hires software and test engineers in Crawley and Helsinki, field service engineers, account managers, manufacturing technicians and finance and HR staff.

Are you a current Elekta employee?

Please click here to apply through our internal career site Find Jobs - Elekta.

We don’t just build technology. We build hope for everyone dealing with Cancer.

Elekta is shaping the standard of care, together with healthcare providers, by developing precision radiation medicine that brings advanced radiotherapy into routine clinical practice. Our solutions support consistent, efficient and personalized care, addressing evolving patient needs. Through adaptive radiotherapy, precision treatment delivery and integrated workflows, Elekta supports care teams across a range of clinical settings. Each year more than 2 million patients are treated using Elekta solutions across over 130 countries. Elekta is headquartered in Stockholm, Sweden, with over 4,000 employees and offices in more than 40 countries. The company is listed on Nasdaq Stockholm. For more information, visit elekta.com.

Product Owner, Treatment Planning Systems (TPS)

What You’ll Do At Elekta

As Product Owner for Treatment Planning Systems (TPS), you will own and prioritize the product backlog in alignment with Elekta’s vision, values and product roadmap. Working closely with Product Management, Development, Engineering, UX, Regulatory, Quality and clinical stakeholders, you will translate customer and clinical needs into clear requirements for Elekta’s treatment planning software and guide development teams through implementation. You will also drive feedback from clinical partners and customers, turning insights from real-world use into product improvements across the product life cycle.

Responsibilities

  • Own and manage the product backlog for the assigned product, ensuring customer and other requirements are planned, designed, implemented and delivered as specified.
  • Partner with Product Management and other Product Owners to understand user needs and formulate customer requirements.
  • Collaborate with Development Teams, Architects and Engineering to create requirements.
  • Work with UX to design user interfaces in line with Elekta design guidelines.
  • Collaborate with Regulatory, Legal and Quality Assurance to incorporate regulatory and quality requirements and provide the input needed throughout development.
  • Drive exploratory testing in clinically relevant environments and scenarios to ensure the product solves the right problems.
  • Analyze, prioritize and incorporate customer and clinical feedback into ongoing development to support high product quality.

What You’ll Bring

  • Bachelor’s degree in medical Radiation Physics, Medical Physics or an equivalent field.
  • At least 3 years of experience in radiotherapy and clinical workflows, gained in a clinical, research or industry setting.
  • Strong knowledge of clinical workflows and radiotherapy treatment planning, such as contouring, dose calculation, plan optimization and evaluation.
  • Experience with regulated medical device software, including quality, risk management, verification and validation.
  • Knowledge of requirements engineering, from user needs through to system requirements, with the ability to write clear, testable requirements and acceptance criteria.
  • Ability to manage and prioritize a product backlog, and to make sound product and design decisions with development teams.
  • Ability to collaborate effectively across Engineering, UX, Regulatory, Quality Assurance and Verification teams, influencing stakeholders without formal line authority.
  • Experience engaging clinical users and translating their feedback into meaningful product improvements.
  • Fluent English and strong communication skills.
  • Hands-on experience using treatment planning systems is preferred.
  • Clinical judgment, customer focus, quality ownership and adaptability in an evolving agile environment.

What You’ll Get

  • Comprehensive occupational healthcare and insurance
  • Accident insurance during work and free-time
  • Lunch benefit
  • Annual sport and culture benefit
  • Mobile phone benefit
  • Flexible working hours to support work-life balance
  • Professional development and learning opportunities
  • 2 additional company-paid days off during the year
  • Modern office in central Helsinki with excellent transport connections
  • An international and collaborative working environment

We believe that great ideas are built together. To support collaboration, team development and innovation, this role is primarily office-based, with an expectation of working from our Helsinki office at least four days per week.

Application process

We look forward to receiving your application. Please submit your CV in English via the “Apply” button. We review applications on an ongoing basis, so we encourage you to apply as soon as possible.

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