Development Quality Engineer

Overview

On Site
$$40.00
Contract - W2
Contract - 1 year

Skills

Testing
Training
Recruiting
Computer Science
Biomedicine
Electronic Engineering
Process Improvement
Regulatory Compliance
Documentation
ISO 9000
Design Controls
Management
Collaboration
Test Plans
Smoke Testing
Mobile Applications
Analytical Skill
Problem Solving
Conflict Resolution
Network
Software Testing
SQL
Database
Verification And Validation
Medical Devices

Job Details

Overview:

(Master's degrees are overqualified), need bachelor's degree in Computer Science, Biomedical Engineer, Electronics Engineering degree.

100 % Onsite.

Will support of Business.

Candidates with exposure in software Verification, validations, and testing (Entry level considered).

Will be working on tickets, troubleshoot and investigate on the tickets.

Working cross functional teams.

Test plans and verify changes request.

Experience with SQL and Databases is huge plus

Software is nice to have, any IT related experience is ok.

High possibilities of extension/conversion.

Will be providing training on 80******** on all these skills, candidates need to be passionate.

Hiring Manager is considering candidates with Medical Device background.

Might consider nonlocal candidates.

Interviews will be virtual followed in person, for non-local candidates might consider virtual interview based on initial interview.

1 year is good, even internship will work.

Computer Science, Biomedical Engineer, Electronics Engineering degree.

What You'll Work On:

Manage projects which may include new production equipment, process improvements and cost reductions while supporting new product introductions.

Work with outside consultants, vendors, and the medical community.

Helps manage Tier II tickets including trouble shooting tickets, clinic creation requests, and other misc. tickets as needed.

Support ad-hoc calls with different sites regarding implementations such as EHR support and setup.

Plan, coordinate, and execute activity in support of project goals.

Establish requirements and specifications.

Identify and mitigate project risks. Helps with Incidence Management including connectivity issues and production issues post deployment.

Ensure compliance with procedural and documentation requirements of client, FDA, and ISO design controls.

Support all Divisional initiatives as identified by divisional management and in support of PPE, RCD, PPG, RCTS, and uality.

Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.

Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Develop test procedures and test plans for lower environment and production deployments.

Assist with EHR courier setup and troubleshooting between client and clinics.

Lead validation and smoke testing on client medical devices and mobile applications.

Troubleshoot Tier II and Tier III tickets escalated by the business and Remote Care Agents.

Strong technical background with an analytical and problem-solving mindset including knowledge of operational deployments requiring network patching, and infrastructure updates.

Required skill

Software Verification

Software Validation

Software Testing

Medical Device

Troubleshooting

Investigating

Changes Request

  • Preferred skills

SQL

Database

1 year of experience in Software Validation/Verifcation on Medical Devices

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