Quality Engineer - DMR Remediation & Transfer

Overview:We are seeking a contract Quality Engineer to support Design Master Record (DMR) remediation and transfer activities as part of the closure of a site. This role will focus on documentation remediation and ensuring quality system compliance during a critical transition period. The ideal candidate is an early-career Quality Engineer or Design Quality Engineer (QE/DQE) with strong attention to detail and experience working within regulated environments.Key Responsibilities:Support DMR remediation activities, including reviewing, updating, and organizing documentation to ensure completeness and complianceAssist with documentation transfer activities related to site closureIdentify gaps in existing documentation and drive remediation effortsCollaborate cross-functionally with engineering, quality, and operations teamsEnsure all documentation aligns with internal quality systems and regulatory requirementsMaintain accurate records and provide updates on remediation progressQualifications:Bachelor’s degree in Engineering or a related technical field1–4 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 processesStrong organizational skills and high attention to detailAbility to work independently in a fast-paced, deadline-driven environmentEffective communication and collaboration skillsPreferred Qualifications:Experience supporting remediation or site transfer/closure activitiesKnowledge of FDA regulations and/or ISO 13485Terms4+ month contractRemote