Jobs at Elekta

Design, develop, and maintain treatment-planning software and features; build high-performance, scalable systems; troubleshoot issues across development, test, and production; reproduce and root-cause customer issues; participate in code reviews; collaborate with global teams; create technical documentation; ensure compliance with QMS and regulatory requirements.

Design, develop, and maintain high-performance, scalable software for treatment planning. Troubleshoot issues across development, testing, and production, collaborate globally, follow coding standards, and ensure QMS and regulatory compliance.

Design, develop, and maintain high-performance treatment-planning software. Troubleshoot and resolve issues across development, test, and production. Collaborate globally, participate in code reviews, produce technical documentation, and ensure compliance with QMS and regulatory requirements while improving development processes and product stability.

As a Senior Software Engineer at Elekta, you will design and develop scalable, cloud-native platforms while mentoring junior engineers, contributing to full-stack development, and improving CI/CD pipelines in a collaborative scrum environment.

This role involves sales and account management for radiation therapy equipment, focusing on strategic sales, new business development, and market analysis in the healthcare sector.

Support the Applications training team with administrative and training tasks: arrange customer travel and accommodation, process meal reimbursements, report monthly KPIs, assist trainers with certificates and preparation, attend in-house trainings, and complete CLM reports/work orders when requested.

Provide expert application support for Elekta Oncology Information Systems (OIS): troubleshoot software issues, document and escalate complex problems, support updates, maintain product knowledge, and travel to customer sites as needed to resolve issues and optimize clinical workflows.

Coordinate order fulfillment and project activities across departments and customers, manage logistics, enter orders and POs into ERP/CRM, maintain project budgets and files, process change orders, invoices and credits, ensure regulatory clearance, and support project lifecycle from initiation to closure.

The Clinical Sales Manager is responsible for engaging with customers, enabling sales, demonstrating clinical expertise, and collaborating across functions to drive sales growth and operational excellence.

Support IP team by identifying and evaluating inventions, conducting prior-art searches and patentability assessments, maintaining patent records, monitoring competitors, and promoting IP awareness across engineering teams.

Provide IP support across patent, trademark, design, copyright and trade secret matters; harvest and assess inventions; draft and prosecute patent applications; advise on third-party IPR risk; train engineering and product teams; oversee outside counsel with Senior IP team support.

The Senior Project Manager / RTE will lead cross-functional teams, ensuring project delivery, compliance with regulatory standards, and effective management of product development activities.

The Regulatory Affairs Specialist will manage regulatory submissions, collaborate with teams, ensure compliance, conduct audits, and drive process improvements.

The Sales Director will represent the organization, develop sales strategies, manage client relationships, oversee financial goals, and ensure compliance with regulations.

Coordinate regulatory block and release activities for products and spare parts; maintain regulatory status in ERP; review release forecasts; provide regulatory guidance for orders and shipments; monitor and report process performance; collaborate with cross-functional teams; identify and implement process and tool improvements; support compliance initiatives and update product catalogue content.

Perform daily corporate accounting tasks including journal entries, reconciliations, month-end close, project revenue recognition, tax report support (VAT/Intrastat), management reporting (cost, revenue, COGS), audit support, stakeholder queries, and process improvement across international entities.

Maintain and improve the Quality Management System for medical device products. Lead quality/compliance activities, monitor metrics, conduct audits, investigate non-conformances, manage CAPA and root cause analyses, approve quality documentation, and partner with cross-functional teams to implement process improvements and ensure regulatory compliance.

Ensure accuracy and synchronization of supply chain and operational data by investigating system issues, monitoring alerts, performing data maintenance, producing reports and dashboards, developing automation and KPIs, documenting processes, supporting global projects, and collaborating with stakeholders to improve data quality and operational performance.

The role involves designing automated test cases, developing reusable automation code, running scripts, and investigating test failures within Agile and Scrum methodologies.

Install, configure, and support MOSAIQ oncology information system integrations with EMRs. Perform software and SQL installations, develop and troubleshoot HL7/C-CDA/FHIR/XML/APIs, create specs and test plans, train service teams, and support migrations and upgrades.