Senior Quality Engineer

Join a highgrowth medical device manufacturer Own impactful work across validation, compliance, and production support About Our Client My client is a global leader in micromanufacturing, 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 Description Ensure 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, nonconformance investigations, complaint handling, change control, and documentation updates. Provide quality engineering support to production, manufacturing engineering, and valuestream activities. Oversee supplier quality activities, including qualification, audits, performance tracking, and crossfunctional 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 Applicant A 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, nonconformance 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 crossfunctionally in a fastpaced setting. Must be proactive, collaborative, organized, and comfortable interfacing with customers and suppliers. What's on Offer Competitive salary ranging from $90,000 to $110,000 USD. Comprehensive benefits package. Support highvolume manufacturing for top global medical device OEMs Strong culture: collaborative, highperforming, 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! Contact Cian Troy Quote job ref JN-022026-6958134

Created: 2026-03-10