Clinical Solution Specialist - Validation & Pilot Release
Posted 12 hours 3 minutes ago by Elekta AB
Permanent
Full Time
Other
Sussex, Crawley, United Kingdom, RH100
Job Description
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. 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. 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%).