ICS is looking for an experienced Quality Engineer who is interested in playing a key role in complex software development projects. The Senior Quality Engineer will define test strategies and develop and execute verification and validation plans. The successful candidate will help drive quality analysis and refine requirements for testability, gaps and clarity.
Contribute as a core team member representing the Quality Engineering functions in activities such as verification and validation planning and risk analysis.
Develop Software Quality Plans and Procedures throughout the software development life cycle.
Experience in developing and executing sophisticated regression, acceptance, integration, performance, load, system-level, and reliability types of testing for all types of systems and platforms
Maintain and comply with ICS/Client SOP’s insuring compliance with the Quality Management System requirements.
6+ years’ experience in quality testing
Expertise in software traceability, defect tracking and metrics
Strong technical writing skills, including development of test plans, procedures, and test reports
Demonstrated experience successfully executing different testing methodologies (Performance, White and Black Box testing
Experience in Agile/Scrum methodology
Regulated or medical device software verification experience
Strong communication and organizational skills
Professional services or consulting environment expertise is preferred
Working knowledge of FDA requirements: ISO 13485, IEC 62304, IEC 60601 and ISO14971
Bachelor’s Degree in Computer Science or relative experience is required