Beschreibung
A Global Medical device company is currently looking for a consultant to work on a Design History File Remediation looking for the last member within their high performing team that reports into the R&D function of the business.Areas in the following Skills and Experience Required
Required experience with CFR 820
Electro-mechanical medical device development
Full lifecycle application development using standard frameworks and coding standards/patterns
Coding, unit testing and debugging applications in various software languages
Software testing and quality assurance
Performance tuning, improvement, balancing, usability, automation
Document software code and ensure that technical documentation i.e. configuration guides, install guides meet requirements
Proactively engage in the remediation of software issues such as code quality, pattern mismatch, and security issues related to the code/configuration
Detailed technical knowledge of techniques, standards and state-of-the art capabilities for authentication and authorization, applied cryptography, security vulnerabilities and remediation
Software development experience
The Position is for an initial 6-month contract with potential extension.