Clinical Solution Specialist – Validation & Pilot Release in Crawley

Want to join a team with a mission to improve and save lives? We continually look for motivated and skilled individuals who are interested in supporting our customers – healthcare professionals who use our products to help patients and their communities. Are you passionate about shaping the future of radiation oncology and ensuring innovative solutions truly meet clinical needs? We are looking for a Clinical Solution Specialist to bring clinical expertise, user insight, and a strong quality mindset into the heart of Elekta’s product development and validation activities.

In this role, you will act as the voice of the clinical user, supporting the validation, testing, and release readiness of Elekta’s solutions while collaborating closely with engineering, product management, and global stakeholders. You will apply your radiation oncology knowledge to influence workflows, treatment techniques, and end‑to‑end user experience, helping to ensure our products are safe, compliant, and clinically meaningful. This is a highly collaborative role that combines hands‑on validation work, clinical review, training, and professional development—ideal for someone who enjoys working at the intersection of clinical practice, technology, and innovation.

What you’ll do at Elekta:

• Perform exploratory and formal validation activities for Elekta product releases.
• Contribute to test design, preparation, execution, documentation, and reporting.
• Ensure all validation work complies with regulatory and quality standards.
• Apply clinical radiation oncology knowledge to support product development.
• Provide clinical insights on workflows, treatment techniques, and user needs.
• Deliver system demonstrations, clinical reviews of prototypes, and workflow evaluations.
• Work with engineering, product management, and other functions during design, development, and testing.
• Participate in workshops, planning sessions, and system demonstrations.
• Support internal training programs and pilot phases.
• Support established Elekta products by delivering new features and assisting with escalated clinical application issues.
• Provide training to Elekta colleagues and contribute to onboarding of new employees.
• Maintain professional registration and continuous professional development.
• Complete required onboarding, process training, and job‑specific qualifications.
• Adhere to Elekta values, Elekta Quality standards, and the Code of Conduct.
• Use effective verbal and written communication to build strong cross‑functional relationships.
• Address necessary topics and manage difficult conversations constructively.
• Take initiative, support team goals, and proactively contribute to assigned work.
• Demonstrate resilience, adaptability, and a positive, solution‑focused attitude.

The right stuff:

• Strong verbal and written communication skills for cross‑functional collaboration.
• Ability to provide clinical input during design, development, and testing phases.
• Skilled in delivering system demonstrations, clinical reviews, and internal training.
• Constructive handling of difficult conversations and cross‑functional challenges.
• Resilience, adaptability, and a proactive, positive attitude.
• Strong organisational skills and ability to manage multiple tasks.
• Commitment to continuous professional development and maintaining professional registration.
• Initiative‑driven approach to learning, contribution, and team support.

What you bring:

• Competence in exploratory and formal validation testing, including test design, preparation, execution, and reporting.
• Understanding of regulatory and quality standards relevant to medical devices and software.
• Ability to assess clinical usability, workflow alignment, and safety considerations.
• Experience with engineering and validation tools such as JIRA, Polarion, and Salesforce.
• Knowledge of Elekta systems such as linear accelerators, XVI, iView, Integrity, MOSAIQ, SmartView, and Monaco TPS (highly desirable).
• Understanding of hardware, software, and solution‑level releases within a medical technology environment.
• Ability to support established products, new features, and pilot deployments.
• Strong analytical thinking and structured problem‑solving abilities.
• Ability to identify clinical risks, workflow gaps, and usability issues.
• Competence in interpreting test outcomes and contributing to release decisions.
• Experience with products from other radiotherapy vendors.
• Exposure to product testing, validation methodologies, and regulatory frameworks.
• Ability to travel domestically and internationally (up to ~35%).

What you’ll get:

In this role, you will work for a higher purpose; hope for everyone dealing with cancer, and for everyone regardless of where in the world, to have access to the best cancer care. In addition to this, Elekta offers a range of benefits.

• Work Pattern (you are required to work from the Crawley HQ 4 days a week with 1 day WFH)
• Up to 25 paid vacation days (plus bank holidays)
• Holiday Purchase Scheme
• Private Medical Insurance
• Attractive Employer Pension Contribution Package
• Cycle to work scheme
• Life Assurance
• Onsite subsidized restaurant, offering budget-friendly dining
• Love electric (Electric vehicle salary sacrifice scheme)

Hiring process:

We are looking forward to hearing from you! Apply by submitting your application and résumé in English, via the “Apply” button. Please note that we do not accept applications by e‑mail.

We are an equal opportunity employer. We evaluate qualified applicants without regard to age, race, colour, religion, sex, sexual orientation, gender identity, genetic information, national origin, disability, veteran status, or any other protected characteristic.