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1 день назад

Product Owner, Treatment Planning Systems (TPS)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
c1
Страна
Finland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Product Owner, Treatment Planning Systems (TPS) (Radiotherapy Software): Owning and prioritizing the product backlog for treatment planning software, translating clinical and customer needs into requirements, and guiding cross-functional development with an accent on radiotherapy workflows, regulated medical device software, and clinical usability. Focus on writing testable requirements, driving exploratory testing in clinically relevant scenarios, and incorporating clinical feedback into high-quality product improvements.

Location: Helsinki, Finland; primarily office-based with an expectation of working from the Helsinki office at least four days per week.

Company

hirify.global develops precision radiation medicine and radiotherapy solutions used by healthcare providers and clinical care teams worldwide.

What you will do

  • Own and prioritize the product backlog for treatment planning systems, ensuring requirements are planned, designed, implemented, and delivered.
  • Translate customer and clinical needs into clear product requirements in collaboration with Product Management and other Product Owners.
  • Collaborate with Development, Architecture, Engineering, UX, Regulatory, Legal, Quality Assurance, and Verification teams throughout development.
  • Guide treatment planning software requirements and user interface design in line with product and design guidelines.
  • Drive exploratory testing in clinically relevant environments and scenarios.
  • Analyze customer and clinical feedback and incorporate it into ongoing product improvements.

Requirements

  • 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, including 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 system requirements, including writing clear, testable requirements and acceptance criteria.
  • Ability to manage and prioritize a product backlog and make sound product and design decisions with development teams.
  • Ability to collaborate across Engineering, UX, Regulatory, Quality Assurance, and Verification teams and influence stakeholders without formal line authority.
  • Experience engaging clinical users and translating their feedback into meaningful product improvements.
  • Fluent English and strong communication skills.
  • Clinical judgment, customer focus, quality ownership, and adaptability in an evolving agile environment.

Nice to have

  • Hands-on experience using treatment planning systems.

Culture & Benefits

  • Comprehensive occupational healthcare and insurance, plus accident insurance during work and free time.
  • Flexible working hours supporting work-life balance.
  • Professional development and learning opportunities.
  • Lunch, mobile phone, annual sport and culture benefits, and two additional company-paid days off.
  • Modern central Helsinki office and an international, collaborative working environment.

Hiring process

  • Submit a CV in English through the application button.
  • Applications are reviewed on an ongoing basis.

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