Vacancy expired!
Description:The R&D Support Technician works in a project team environment supporting test planning, test script development, test script execution and regression testing with accompanying documentation for medical and biopharma diagnostic devices. This individual also helps in the development of requirements, FMEAs and ECO processing while supporting R&D Engineers and Documentation Control personnel. Performs both manual and automated testing strategies on medical device systems and biopharma diagnostic devices. Responsible for correct and complete documentation of verification and validation methods. Evaluates software applications for errors and stability. Debugs test scripts and identifies system flaws. Develops testing strategies and analysis for software programs. Reviews functional specifications, design documents, and other development documents to gain understanding of features and requirements to aid in the development of test protocols. Develops and maintains test plans, test specifications and test protocols for features and products. Participates in reviews of software design and coding. Ensures all developed test protocols follow testing standards and are appropriately documented. Interacts with Hardware/Software Engineers to ensure currently assigned tasks are prioritized appropriately and to define, create and improve verification procedures and methods. Participates in the development and maintenance of system requirements, FMEAs and ECOs. Must be self-motivated, capable of working independently and able to work in team environment. Assists with organizing outside testing, reviews, reports and provides administrative support as needed. Maintains equipment, test configurations and databases of clinical data used for verification and validation testing.Skills:testing, verification, validation, V&V, documentation, quality assurance, Debugging, fmea, ECO, I2C, SPI, GMP, Medical Device, ISO, Diagnostics, hardware, pumps, mechanical system, software, firmware, R&D, reseach and development, Test execution, trouble shootingTop Skills Details:testing,verification,validation,V&V,documentation,quality assuranceAdditional Skills & Qualifications: 1-7 years’ experience in testing, troubleshooting and developing complex devices and systems. Experience in Medical Device, GMP or Diagnostics Equipment environment preferred. Familiar with software engineering tools (Debuggers, I2C, SPI, etc.). Ability to document requirements and specifications. Proficient in MS Office (MS Word and Excel). Strong troubleshooting and problem solving abilities. Excellent oral and written communication skills required.Experience Level:Intermediate LevelAbout Actalent: Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Vacancy expired!