Save Job Back to Search Job Description Summary Similar JobsLead complex quality initiativesStep into a senior, hands‑on roleAbout Our ClientThis organisation is a well‑established, multi‑site manufacturing business supporting technically complex products across a range of regulated and industrial markets. They are known for strong in‑house capabilities, a safety‑first culture and a genuine commitment to continuous improvement.Job DescriptionLead the design, documentation and implementation of advanced process controls, SPC, inspection and testing methodologies.Drive root cause analysis for complex quality issues using structured problem‑solving tools and ensure effective corrective and preventive actions.Manage and lead large, cross‑functional quality and process improvement projects, ensuring timelines, resources and communication are aligned.Conduct and lead internal quality system audits to support ongoing compliance and system improvement.Facilitate and lead CAPA activities, including meetings, action tracking and verification of effectiveness.Lead APQP activities to ensure robust product and process validation and verification.Develop, maintain and analyse quality system metrics to support data‑driven decision making.Partner with engineering teams to leverage historical performance data and proactively prevent recurrence of quality issues.Apply advanced quality and engineering tools such as DOE, DFM, FMEA, GD&T, process capability analysis and Six Sigma methodologies.Act as a key member of the Material Review Board, supporting failure analysis and disposition decisions.Lead and develop blueprint reading and quality training programmes for new hires and ongoing employee development in partnership with HR.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.The Successful Applicant5-7 years of recent, relevant experience in a manufacturing environment.Strong hands‑on understanding of manufacturing processes, tooling and production controls.Solid working knowledge of ISO 9001 quality systems; internal or external auditing experience preferred.Experience with medical systems and ISO 13485 audits is highly desirable.Bachelor's degree in Engineering and/or Certified Quality Engineer (CQE) preferred.What's on OfferSenior‑level opportunity with real impact on site‑wide quality performanceExposure to complex manufacturing processes across multiple industriesStrong safety‑first, accountability‑driven cultureCompetitive total rewards package including bonus, 401(k) match and education supportStable, growing organisation that invests in technical leadership and career developmentContactBridget PettiQuote job refJN-052026-7018151Job summarySectorEngineering & ManufacturingSub SectorQuality, TechnicalIndustryIndustrial / ManufacturingLocationSpringfieldContract TypePermanentConsultant nameBridget PettiJob ReferenceJN-052026-7018151