Verification & Validation Engineer I

Envista Holdings Corporation•Quakertown, PA

1d•$79,800 - $94,500•Hybrid

About The Position

DEXIS is looking for individuals who work their best, help others, and commit to helping us improve our customer lives and celebrate the difference in others. We are the leading manufacturer and distributor of innovative dental imaging equipment, software, and solutions. We offer meaningful work through innovation, diverse opportunities, and career progression. The Quakertown facility is our North American hub for the design and manufacturing of leading dental imaging devices and software. The facility has a growing, energetic, and diverse mix of professionals spanning engineering, operations, regulatory and quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open atmosphere helps to foster strong personal and professional relationships across the organization. The V&V Engineer I will utilize experience to lead and execute formal verification and/or validation planning and testing for our DEXIS software. Projects include a broad range of dental imaging software products with hardware interfaces and associated support software. The candidate will work closely within a core team of Software, Hardware and V&V Engineers dedicated to the development and continuous improvement of products.

Requirements

Bachelor’s degree in an Engineering / Technical field or 2+ years(s) equivalent work experience.
Knowledge of testing methodologies (ex. software testing)
Ability to troubleshoot applications and identify root causes of defects.
Comfortable managing priorities and timelines.
Detail-orientated with a focus on accuracy and quality.
Ability to track testing progress and ensure completion
Strong understanding of Windows OS environments
Must be able to work on-site 4 days per week with one day remote.

Nice To Haves

Experience developing verification test cases, procedures, plans, analyzing test results, and writing reports.
Experience on setting up computer workstations and deploying software onto target systems and/or virtual machines.
Experience in system-level verification testing in a regulated industry; experience in a medical device industry (21 CFR Part 820.30, ISO13485) preferred.
Knowledge of Medical Device/FDA Regulated Industry and compliance with IEC-60601, 62304, ISO14971, IEC 62366, EU MDR preferred.
Experience with requirements management (including technical content reviews), design reviews, test reviews, and change control activities.
Experience using Requirements, Test Case and Incident Management tools (e.g. – Jama, DOORS, JIRA).
Hands-on experience with designing, building, and maintaining test fixtures and/or working with external laboratories to perform testing.

Responsibilities

Performs verification testing, tracks and reports on progress, documents incidents found, ensure test completion, reviews results, and generates reports.
Performs testing on various Windows software programs and hardware devices developed by the company.
Communicates with Engineering to identify root causes of test failures, evaluate mitigations and re-test new versions.
Tests software/hardware integration of dental imaging x-ray equipment.
Tests cloud based IoT telemetry, installation, and software updates.
Troubleshoots custom Windows applications (installation, permissions, services, conflicts, general inner workings of Windows).
Configures, updates, manages, and re-images Windows based computers and Virtual Machines used for testing.
Develops, reviews and executes test cases and procedures.
Participates in the planning and lead the execution of verification testing activities in support of assigned projects.
Coordinates with other Verification Engineers on assigned tasks.
Works closely with all engineering disciplines and RA/QA personnel.
Assists with development of test systems, environments, and fixtures.
Completes other duties as assigned.