Quality Systems Analyst

Quality Systems AnalystLocation: Irvine, CASchedule: StandardDuration: 9 Month ContractPay Range: $40.50-45.55/hr Summary:The Quality Systems Analyst supports execution of Supplier Quality documentation remediation activities, including outreach, negotiation, and completion of Quality Agreements with external suppliers. This role serves as a primary point of contact for suppliers, working to secure agreement on quality system requirements while ensuring timely issue escalation and closure. Job Responsibilities:In this role, you will manage and support a variety of projects within the Supplier Quality department. Key responsibilities include:Executing supplier outreach and managing a portfolio of Quality AgreementsCommunicating Quality System and regulatory requirements to suppliers and addressing routine questions or concernsNegotiating language within established guidelines and identifying issues requiring escalationCollaborating with Supplier Quality, Sourcing, Legal, and business stakeholders to resolve supplier objections and drive executionMaintaining project documentation, supplier communication records, status reporting, and metrics to support leadership visibility and program execution Essential Job Duties and Job Functions:Own and progress a portfolio of active Quality Agreements from outreach through executionServe as the primary supplier point of contact for quality documentation mattersEscalate unresolved supplier objections or high-risk issues in a timely mannerTrack and report status/metrics to leadership on a regular cadence Knowledge and Skills:Experience in a quality and/or manufacturing environment in the medical device industry requiredProven expertise in MS Office SuiteGood project management skills and related software tools preferredExcellent written and verbal communication skills, including negotiation and relationship managementStrong problem-solving and critical thinking skills Education and Experience:Bachelor's Degree or equivalent in a related field of studyExperience in a quality and/or manufacturing environment in the medical device industry required2-4 years of experience required...