Lead Software Test Engineer (Manual - Onsite in Durham, NC)

Fujifilm•Durham, NC

1d•Onsite

About The Position

This position is intended to conduct manual and tool assisted testing of new and existing features in medical device software systems. Coordinates and reviews the testing activities of other members of an agile team. At FUJIFILM Healthcare Americas Corporation, we’re on a mission to innovate for a healthier world, and we need passionate, driven people like you to help us get there. Our cutting-edge healthcare solutions span diagnostic imaging, enterprise imaging, endoscopic and surgical imaging, as well as in-vitro diagnostics. But we don’t stop at healthcare; our Non-Destructive Testing (NDT) team harnesses advanced radiography solutions to keep transportation infrastructure, aerospace, and oil and gas assets safe and running smoothly. Ready to innovate, collaborate, and make a difference? Join us and bring your big ideas to life while working in a dynamic, flexible environment that fuels your creativity and drive. Our headquarters is in Lexington, Massachusetts, an inspiring healthcare research hub in a historic town. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers

Requirements

BS degree or higher in a scientific, engineering, or clinical field.
Feature level QA responsibility, including providing test leadership.
Basic coding/scripting skills.
Experience working on and understanding of large, complex systems.
Experience working in a regulated industry, preferably software medical device.
Testing experience in agile environments.
Knowledge of web software, network and IT, medical devices, regulated environments.
Working knowledge of DICOM, HL7, SQL, Oracle, IIS, scripting, JavaScript, TFS, MTM, PACS.
Good verbal and written communication skills.
Determination to obtain results.
Passionate about using technology to innovate, in order to deliver the best clinician and patient experience.
Enjoys working in a team and vice-versa.
Ability to handle fluctuating workloads.
Able to see the big picture as well perform detailed analyses.
Self-directed and goal oriented.
Awareness of and advocate for industry best practices.
Able to guide QA team members.

Responsibilities

Coordinate and review the testing activities of other members of an agile team.
Provide estimates and status to management while preparing for the System Test phase of a project/release.
Create regression testing plan and monitor the execution during the System Test phase.
Coordinate the creation of automated regression tests or instructions for automation, as per the team’s definition of done.
Coordinate the development/enhancement of a model of the system components that the team works on.
Understand the scope/requirements of the project from requirements, user stories and interactions with the team.
Identify conceptual/design/requirements and software issues in early stage of testing and actively follow-up until resolved.
Create, modify, and execute exploratory test scenarios, with the goal of maximizing early defect discovery and eliminating issues discovered later.
Create or modify and execute test cases.
Create or modify test data.
Develop test tool or use off the shelf tools to increase productivity.
Define scope and objectives for various test activities.
Develop, implement, and review the test plans.
Responsible for coordinating testing for projects.
Report status and escalate issues effectively.
Verify the accuracy of the product documentation.
Coach and mentor less experienced team members in testing best practices.
Add value in a team environment consisting of cross-functional members.
Identify process improvements to increase the performance, productivity and consistency of testing.
Strong interpersonal / communication skills to be able to work with various teams in the organization.
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.