Save Job Back to Search Job Description Summary Similar JobsJoin a high‑growth medical device manufacturerOwn impactful work across validation, compliance, and production supportAbout Our ClientMy client is a global leader in micro‑manufacturing, laser processing, and medical device component production, serving top-tier customers. The New Hampshire site is ISO 13485 and 21 CFR-compliant, operating with over 100 employees and a culture known for high performance, collaboration, and strong leadership.Job DescriptionEnsure compliance with ISO 13485, 21 CFR 820, and Quality Systems across all development and production activities.Lead validation protocols, risk assessments, design control documentation, DHF/DMR creation, and statistically designed experiments.Manage CAPA, non‑conformance investigations, complaint handling, change control, and documentation updates.Provide quality engineering support to production, manufacturing engineering, and value‑stream activities.Oversee supplier quality activities, including qualification, audits, performance tracking, and cross‑functional communication.Develop inspection/quality plans, sampling strategies, and maintain QMS processes including training, equipment calibration, and document control.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.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 ApplicantA successful Senior Quality Engineer should have:Bachelor's degree with 5+ years of Quality Engineering experience (medical device strongly preferred).Experience with ISO 13485, 21 CFR 820, risk management, validations, and design control processes.Strong background in CAPA, non‑conformance management, supplier quality, and QMS execution.Proficiency in statistical tools, sampling plans, Gage R&R, and process analysis.Ability to manage multiple projects, communicate effectively, and work cross‑functionally in a fast‑paced setting.Must be proactive, collaborative, organized, and comfortable interfacing with customers and suppliers.What's on OfferCompetitive salary ranging from $90,000 to $110,000 USD.Comprehensive benefits package.Support high‑volume manufacturing for top global medical device OEMsStrong culture: collaborative, high‑performing, and well supported by leadership.Broad exposure to manufacturing, engineering, audits, supplier quality, and QMS ownership.Growing site with high project diversity and strong investment in people and processes.If you are passionate about quality engineering and are eager to contribute to the Medical Device industry, I encourage you to apply today!ContactCian TroyQuote job refJN-022026-6958134Job summarySectorEngineering & ManufacturingSub SectorQuality, TechnicalIndustryIndustrial / ManufacturingLocationHudsonContract TypePermanentConsultant nameCian TroyJob ReferenceJN-022026-6958134
