Senior Software System Engineer

Elekta AB

Veenendaal

On-site

EUR 90,000 - 120,000

Full time

6 days ago
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Job summary

Elekta AB in the Netherlands is seeking a senior engineer to lead and maintain requirements, specifications and R&D documentation for medical device software development. You will define design inputs based on user needs, customer requirements, usability goals, and applicable standards and regulations.

Responsibilities include structuring system requirements and test specifications, ensuring cyber security compliance, managing risk management activities, and guiding cross-functional teams from

Qualifications

  • 7+ years of recent work experience with system engineering or requirements engineering for software products in a regulated industry, preferably medical devices.
  • Experience with lean-agile-scrum way of working and Polarion.
  • Knowledge on the cyber security lifecycle (IEC 8100-5-1) and the FDA cybersecurity in Medical Devices guidance.
  • Knowledge of regulations, standards and risk management, preferably EU 2017/745 (MDR), IEC 62304, ISO 13485 and ISO 14971.

Responsibilities

  • Structure, define and review design input requirements (based on user needs, customer requirements, usability goals, standards & regulations, etc.).
  • Structure, define and review (sub-) system requirements and test specifications for software development, product development and maintenance (e.g. functional requirements, performance requirements, risk control measures, etc.).
  • Keep the products compliant regarding the latest cyber security standards.
  • Contribute to risk management, usability engineering, and the continuous improvement of the Design & Development Files and our processes and tools.
  • Knowledge transfer to software architects, software engineers and other disciplines involved in product development (e.g. Product Mgt., QA-RA, system verification, validation, project leads, etc.).
  • Participate in roadmap discussion. Oversee the needs of the different stakeholders, including engineering.
  • Manage the backlog from a Product Owner perspective
  • Manage the change control of software change requests and defects

Skills

Lean-Agile-Scrum
Cyber security
Clear communication

Education

Bachelor's degree in Computer Science

Tools

Polarion

Job description

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.

Description Leading role in creating and maintaining requirements, specifications and R&D documentation for medical device development
Responsibilities
  • Structure, define and review design input requirements (based at e.g. user needs, customer requirements, usability goals, standards & regulations, etc.)
  • Structure, define and review (sub-) system requirements and test specifications for software development, product development and maintenance (e.g. functional requirements., (essential) performance requirements., risk control measures, etc.)
  • Keep the products compliant regarding the latest cyber security standards.
  • Contribute to risk management, usability engineering, and the continuous improvement of the Design & Development Files and our processes and tools.
  • Knowledge transfer to software architects, software engineers and other disciplines involved in product development (e.g. Product Mgt., QA-RA, system verification, validation, project leads, etc.)
  • Participate in roadmap discussion. Oversee the needs of the different stakeholders, including engineering.
  • Manage the backlog from a Product Owner perspective
  • Manage the change control of software change requests and defects
Authorities
  • Accountable for the requirements of the Brachy Solutions software.
  • Accountable for the compliance to standards, including cyber security, of the Brachy Solutions software.
  • Accountable for the completeness of the backlog for a release project and the maintenance activities
Relevant Knowledge, skills and competencies
Formal Education:
  • At least a bachelor’s degree in computer science or comparable.
Experience & Knowledge:
  • At least 7 years’ recent work experience with system engineering or requirements engineering for software related products in a regulated industry, preferably medical devices.
  • Experience with lean-agile-scrum way of working and with well-known requirements engineering software, preferably Polarion.
  • Knowledge on the cyber security lifecycle (IEC 8100-5-1) and the FDA cybersecurity in Medical Devices guidance
  • Knowledge of regulations, standards and risk management, preferably EU 2017/745 (MDR), IEC 62304, ISO 13485 and ISO 14971.
Personal attributes:
  • Being able to communicate on a clear way, using good listening, speaking and writing skills, in English and preferable in Dutch
  • Accurate and good analytical and problem-solving skills.
  • Team player, but also very capable of working independently.
  • Proactive attitude; actively focused on achieving results.
About Elekta

As a leader in precision radiation therapy, Elekta is committed to ensuring every patient has access to the best cancer care possible. We openly collaborate with customers to advance sustainable, outcome-driven and cost-efficient solutions to meet evolving patient needs, improve lives and bring hope to everyone dealing with cancer. To us, it's personal, and our global team of 4,700 employees combine passion, science, and imagination to profoundly change cancer care. We don’t just build technology, we build hope. Elekta is headquartered in Stockholm, Sweden, with offices in more than 120 countries and listed on Nasdaq Stockholm. For more information, visit elekta.com or follow us on LinkedIn, Glassdoor, Twitter, Facebook, Instagram and YouTube.

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