Quality Engineer [80368]

Onward Search is a specialized staffing and talent solutions company that helps professionals find top jobs with the nation’s leading brands. We’re hiring a Quality Engineer for an onsite role in Savannah, Georgia.Join our client’s team at their Savannah location, where you will play a pivotal role in ensuring quality excellence and regulatory compliance within a dynamic manufacturing environment focused on dental and orthopedic instrumentation.This is a 6-month contract opportunity with the possibility of extension. This role requires an onsite presence 5 days per week. Onward Search provides benefits for a 40-hour work week and weekly paychecks (W2) for the duration of the contract.There is no application deadline for this role.* No sponsorship and no relocation reimbursement * Pay: $100 - $110 / hour W2* 6 month contract + extension* Location of team: Savannah, GA* On-site 5 days/week * Onward Search provides benefits and weekly paychecks (W2)Quality Engineer Responsibilities:Spearhead the remediation of technical files in alignment with EU MDR requirements, preparing comprehensive submissions for the notified body.Lead investigations into Corrective and Preventive Actions (CAPA) and Nonconformance issues, ensuring effective trend analysis, containment, correction, and verification.Enhance and sustain the Quality Management System (QMS) by managing complaints, contributing to management review inputs and metrics, and refining process controls.Collaborate with engineering teams to support design controls and risk management activities.Engage in ISO 13485 and MDSAP compliance initiatives, providing support during audits as necessary.Work closely with manufacturing teams, primarily from an office setting, with occasional on-site floor support.Quality Engineer Qualifications:A robust professional background, with 7–10+ years of relevant experience, is preferred.Proven experience in the medical device industry, specifically within a Quality Engineering or Quality Management System capacity for Class I/II devices.Demonstrated expertise in EU MDR remediation and the development of technical files.In-depth knowledge of ISO 13485, MDSAP, CAPA/NC processes, and design-control principles.Ability to work independently in a fast-paced, multi-shift manufacturing environment, with a required on-site presence.Familiarity with orthopedic instrumentation and dental device products (preferred).Experience in site consolidations, technology transfers, and supplier quality audits (preferred).Perks & Benefits:Medical, Dental, and Vision Insurance.Life Insurance.401(k) Program.Commuter Benefit.eLearning & Ongoing Training.Education Reimbursement.*Eligibility requires working over 30 hours per week on an assignment lasting at least 10 weeks.If you meet the qualifications and are excited about this opportunity, apply today! Our team will connect with you to discuss next steps, support you through the interview process, and advocate for your success.