QA Analyst with Medical Devices

01 Dec 2024

Vacancy expired!

Must HaveBachelors DegreeC#Google DocsHTMLHTTPImaging system QA experienceJavaScriptMatLabMicrosoft PowerPointMicrosoft VisioMicrosoft WordMS Visual Studio.NETPythonTypeScriptWeb Development

Nice To HaveCDICOMGoHL7Masters DegreePACSPython ProgrammingRecent grads with degrees in BME or CS preferred from Duke, UNC, NC State. Medical Device, gaming software, imaging experience a plus. Mostly a remote position but needs to be local in order to use the lab for performance testing. Duties and Responsibilities:
  • Coordinate and review the testing activities in an agile software development team, including an understanding of the team’s definition of done.
  • Drive the creation of regression tests, using automation where feasible.
  • Understand the scope/requirements of the project from requirements, user stories and interactions with the team.
  • Identify conceptual/design/requirements and software issues at an early stage of testing and actively follow-up until resolved.
  • Report status and escalate issues effectively.
  • Define scope and objectives for various test activities.
  • Create or modify and execute test cases.
  • Create or modify test data.
  • Develop test tools or use off the shelf tools to increase productivity.
  • Develop, implement and review the test plans.
  • Coordinate the development/enhancement of a model of the system components that the team works on.
  • Set up and configure the application’s test environment from scratch, including operating system and application installation, virtual machine management.
  • Provide estimates and status to management for the System Test phase of a project/release.
  • Create regression testing plan and manage the test execution during the System Test phase.
  • Create, modify and execute exploratory test scenarios, with the goal of maximizing early defect discovery and eliminating late discovery of issues.
  • Verify the accuracy of the product documentation.
  • Coach and mentor less experienced team members in testing best practices.
  • Identify process improvements to increase the performance, productivity and consistency of testing.
  • Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations and standards.

Qualifications:
  • BS degree or higher in a scientific, engineering or clinical field.
  • 2-5 years of experience in software development.
  • Feature level QA responsibility, including demonstrated test leadership.
  • Extremely strong interpersonal / communication skills, both verbal and written.
  • Basic coding/scripting skills.
  • Experience working on, and understanding of, large, complex systems.
  • Experience working in a regulated industry, preferably software medical devices.
  • Testing experience in agile environments.
  • Knowledge of web software, network and IT, medical devices, regulated environments.
  • Performing testing using Microsoft products such as TFS, MTM.
  • Working knowledge of DICOM, HL7, SQL, Oracle, IIS, scripting, JavaScript, TFS, PACS.
  • Determination to obtain results.
  • Passionate about using technology to innovate, in order to deliver the best clinician and patient experience
  • Enjoy working in a team.
  • Able to handle fluctuating workloads.
  • Able to see the big picture as well as perform detailed analyses.
  • Self-directed and goal oriented.
  • Awareness of, and advocate for, industry best practices.
  • Able to guide other QA team members.

  • ID: #23705252
  • State: North Carolina Morrisville 27560 Morrisville USA
  • City: Morrisville
  • Salary: Depends on Experience
  • Job type: Contract
  • Showed: 2021-12-01
  • Deadline: 2022-01-28
  • Category: Et cetera