[Remote] Quality Engineer – DMR Remediation & Transfer

GForce Life Sciences
Washington, US
Remote

Job Description

Note: The job is a remote job and is open to candidates in USA. GForce Life Sciences is seeking a contract Quality Engineer to support Design Master Record (DMR) remediation and transfer activities during a site closure. The role focuses on documentation remediation and ensuring quality system compliance, requiring strong attention to detail and experience in regulated environments.

Responsibilities

  • Support DMR remediation activities, including reviewing, updating, and organizing documentation to ensure completeness and compliance
  • Assist with documentation transfer activities related to site closure
  • Identify gaps in existing documentation and drive remediation efforts
  • Collaborate cross-functionally with engineering, quality, and operations teams
  • Ensure all documentation aligns with internal quality systems and regulatory requirements
  • Maintain accurate records and provide updates on remediation progress

Skills

  • Bachelor's degree in Engineering or a related technical field
  • 1–4 years of experience in Quality Engineering or Design Quality within a regulated industry (medical device preferred)
  • Familiarity with Design Master Records (DMR) and documentation control processes
  • Strong organizational skills and high attention to detail
  • Ability to work independently in a fast-paced, deadline-driven environment
  • Effective communication and collaboration skills
  • Experience supporting remediation or site transfer/closure activities
  • Knowledge of FDA regulations and/or ISO 13485

Company Overview

  • GForce Life Sciences is a platform for career management that offers executive search, medical affairs consulting, and project management. It was founded in 2013, and is headquartered in Chicago, Illinois, USA, with a workforce of 51-200 employees. Its website is https://www.gforcelifesciences.com.

Company H1B Sponsorship

  • GForce Life Sciences has a track record of offering H1B sponsorships, with 1 in 2026, 1 in 2024, 1 in 2023, 1 in 2022. Please note that this does not guarantee sponsorship for this specific role.

Skills & Requirements

Technical Skills

Quality engineeringDesign qualityDesign master records (dmr)Documentation control processesFda regulationsIso 13485Organizational skillsAttention to detailIndependent workFast-paced environmentCommunicationCollaborationHealthcare

Employment Type

CONTRACT

Level

mid

Posted

4/16/2026

Apply Now

You will be redirected to GForce Life Sciences's application portal.