6 of 6 Permanent Validation Jobs in West London

acute care organisations or equivalent Experience of Intersystems HealthConnect. Experience developing integration solutions with HL7, Webservices/XML, Files. Experience in implementing data validation and verification solutions to enhance data integrity and quality. Desirable Experience in the transformation of NHS datasets for differing Experience of Acute Hospital Information Systems ...

planning, technical direction, mentoring, and code reviews Collaborate closely with hardware, systems, and manufacturing teams to support board bring-up, debugging, integration, and system validation Own key architectural decisions, helping define software frameworks, coding standards, development processes, and long-term platform strategy Design, implement, test, and maintain embedded software ...

programming concepts and idiomatic Scala (immutability, monads; familiarity with Cats or Scalaz is a plus). Experience designing and consuming REST APIs , including JSON validation/serialization (Play JSON, Circe). Proficiency with relational databases (PostgreSQL) and/or NoSQL (MongoDB), including schema design and query optimization. Proven experience writing ...

Develop high-quality embedded software that is efficient, maintainable, and scalable Work collaboratively with hardware engineers to support board bring-up, debugging, and system validation Design, implement, test, and support embedded software for internally developed electric systems Investigate and resolve complex real-time challenges related to timing, performance, and signal ...

explain the technical mechanics of the vulnerabilities (e.g., XSS, SQLi, CSRF), and guide them on how to fix them at the code level. Remediation Validation : Technically validate and test that the remediations applied by the development team are effective and secure. Secure SDLC Implementation : Embed secure design principles and application ...

hands-on Quality Engineer role where youll play a key part in maintaining and improving an ISO 13485 QMS while supporting product development, validation, and regulatory activities ahead of major commercial launches. What youll be doing: Own and maintain the QMS (ISO 13485) Manage document control, CAPAs, and change control … Support NPD, validation, and testing activities Conduct internal audits and support external/regulatory audits Work closely with engineering and clinical teams What were looking for: 2+ years in medical device quality Strong knowledge of ISO 13485, MDR, and/or 21 CFR 820 Experience with design controls & risk management ...