scarlet - Software Safety Engineer
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Requirements
• Education - A degree in computer science or related discipline • Work experience - Minimum of four years experience in the field of healthcare products or related activities, such as in manufacturing, auditing or research • Work experience - Minimum of two years in the design, development or testing of medical device software (or other critical software) • Work experience - Practical experience in conducting performance, verification and validation testing and/ or assessing performance, verification and validation test protocols, data and results for medical device software • Work experience - Practical experience in programming, demonstrating knowledge of one or more programming languages, software testing and debugging techniques • Work experience - Knowledge of the fundamental principles of programming, software development life-cycle processes, software verification and validation testing, software configuration management and problem resolution techniques along with medical device cybersecurity, interaction between medical software and its environment and data protection • Ferociously curious - You like going down rabbit holes, understanding deeply how things work, and challenging the status quo • Excellent communicator - You have exceptional written & verbal communication skills • Highly adaptable - You have worked in different environments and like operating with autonomy on sometimes ambiguous tasks • Guidance knowledge - You have knowledge or training in the relevant standards and guidance relevant for medical device software (e.g. IEC 62304, IEC 81001-5-1) • AI fluent - You have strong technical knowledge of modern generative AI (e.g., LLMs, embeddings, RAG, fine-tuning, evaluation/monitoring) and have a rich understanding of how these systems work - and where they fail • THE INTERVIEW PROCESS • 1. Intro chat with Hann https://www.linkedin.com/in/hann-yee-son-26101624a/ - 20 mins • 2. Interview with Sandy https://www.linkedin.com/in/wrightsandy/ and a member of the Devices function - 30 mins each • 3. Technical task & interview with Hann https://www.linkedin.com/in/hann-yee-son-26101624a/ - 1 hour • 4. Culture and values interview with James https://www.linkedin.com/in/james-dewar-78758992/?originalSubdomain=uk and Jamie https://www.linkedin.com/in/jamie-cox-01458b3a/?originalSubdomain=uk - 30 mins each • 5. Referencing & offer
Responsibilities
• Get authorised to assess the software lifecycle processes of the most innovative medical devices in the world • Collaborate with a multidisciplinary team on technical documentation assessments • Create content to help explain complex regulatory topics to customers and prospects • Screen and action regulatory insights from the latest research, standards and guidance • Support the Sales and Customer Experience function by providing regulatory insights on prospects and customers • Work with our Product, Engineering, Design and Applied ML functions to build and improve our systems • Support the Technical Operations function as they expand Scarlet’s approvals in various jurisdictions and technologies
Benefits
• £75K – £85K • Offers Equity • Upload your resume here to autofill key application fields. • Drop your resume here! • Parsing your resume. Autofilling key fields... • or drag and drop here • Where are you currently based?
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