125 quality systems engineer jobs at 75 companies in Everett, MA
🚀PromotedHiringCafe
Founding Backend / Infra Engineer
Cupertino, CA, US
$160k-$300k/yrOn-SiteFull Time
HiringCafe: Building a 100× better job search engine to take on Indeed and LinkedIn.
Own the crawlers, pipelines, and infrastructure powering a real-time job search engine. Strong Node.js and Python fundamentals; bonus points for security and reverse-engineering chops.
TTM TechnologiesNASDAQ: TTMI: Manufactures printed circuit boards and radio frequency technology solutions.
8+ YOEMaintain and improve QMS, lead internal/external audits, assess risks, drive corrective actions; Bachelor's degree in engineering/quality/manufacturing or related; 8+ years experience (6+ with Master's); proficiency with Microsoft Office and quality software.
Boston ScientificNYSE: BSX: Developer and manufacturer of innovative medical devices and therapies.
5+ YOEBachelor's degree in engineering/quality/life sciences, 5+ years quality systems experience in a regulated industry, knowledge of ISO 13485/21 CFR Part 820/EU MDR, digital quality systems support, audits, CAPA, and cross-functional collaboration.
VulcanForms: Provides industrial-scale metal additive manufacturing and precision machining services.
3+ YOE3+ years in medical device or aerospace quality with knowledge of FDA requirements, ISO 13485/AS9100/ISO9001, QMS, CAPA, NCR, document control, procedure writing, audits, and quality metrics/KPIs.
Sirtex Medical: Manufactures targeted radiation therapies for inoperable liver cancer patients.
5+ YOEBachelor's in engineering/life sciences required, 5+ years quality systems experience in medical device/pharma/biotech, proven eQMS administration (Veeva, MasterControl, ETQ, TrackWise), and strong knowledge of 21 CFR Part 820, ISO 13485, MDSAP.
Veeva Vault, MasterControl, ETQ, TrackWise, eQMS, Power BI, Tableau, Microsoft Excel
Boston ScientificNYSE: BSX: Manufacturer of interventional medical devices and technologies.
5+ YOEBachelor's degree required, 5+ years in quality systems in a regulated industry, knowledge of ISO 13485/21 CFR Part 820/EU MDR, experience with digital quality systems, audits, CAPA, and cross-functional collaboration.
Access Vascular: Develops biomaterial catheters that reduce clinical complications during intravenous therapy.
5+ YOEBachelor's in Engineering or Life Sciences; 5+ years quality systems in medical devices; QMS experience (FDA 21 CFR Part 820, ISO 13485); CAPA, document control, audits; CQE/CMDA or ISO Lead Auditor a plus.
Senior Quality Systems Engineer (Marlborough, MA, US, 01752)
Marlborough or Arden Hills or Maple Grove
$89k-$170k/yrHybridFull Time
Boston ScientificNYSE: BSX: Developing and manufacturing innovative medical devices for less-invasive treatments.
5+ YOEBachelor's in engineering/quality/life sciences, 5+ years quality systems experience in a regulated industry, knowledge of ISO 13485/21 CFR 820/EU MDR, digital quality systems experience, audit/CAPA support, and process ownership.
TE ConnectivityNYSE: TEL: Manufacturer of electronic connectors and sensors for global industries.
5+ YOEBachelor's in engineering/science or related, 5+ years related experience, ISO 13485 knowledge, audit and CAPA experience, eQMS experience, strong investigation and communication skills.
Senior Systems Quality Engineer (Teradyne, N. Reading MA)
North Reading, Massachusetts, United States
$127k-$207k/yrOnsiteFull Time
TeradyneNASDAQ: TER: Designs and manufactures automated test equipment and advanced robotics systems.
10+ YOE10+ years in quality/systems/test engineering, bachelor's or master's in a technical discipline, strong system validation, automated test framework development, programming and CI/CD experience.
Quality Systems Engineer – CAPA and Process Improvement
Manchester, New Hampshire, United States
OnsiteFull Time
DEKA Research & Development: Designs and develops advanced medical and robotic technologies.
3+ YOEBS/MS in engineering, life sciences, or related field; 3+ years in quality systems in a regulated industry (medical device preferred); working knowledge of FDA QSR (21 CFR Part 820) and ISO 13485; strong technical writing and communication; proficiency with Microsoft Excel, Word, and Visio.
Vor BioNASDAQ: VOR: Developing targeted therapies for chronic autoimmune diseases.
3+ YOE3+ years in GxP quality systems with hands-on eDMS/eQMS/LMS experience, Bachelor's in life sciences or engineering, knowledge of FDA/EMA/ICH requirements, training and document management, and cross-functional collaboration.
Haigh-Farr: Designs and manufactures flight-body antennas for aerospace and defense.
5+ YOEQuality Engineer with AS-9100, 5+ years, BS Mechanical, US Citizenship, ability to obtain security clearance; proficient with GD&T, CMM, and quality systems.
Principal Software Systems Quality Engineer onsite Tewksbury, MA
Tewksbury or Andover or Pelham or Marlborough
$108k-$205k/yrOnsiteFull Time
RTXNYSE: RTX: Provides advanced aerospace and defense systems and services.
8+ YOEU.S. citizenship and ability to obtain/maintain DoD Secret clearance; Bachelor’s in STEM and ~8 years quality/engineering experience; knowledge of Agile, testing, requirements, software lifecycle, metrics, and root cause analysis.
Windchill PDM, Azure DevOps, Azure DevOps Server, Business Insight, Jira, Microsoft Excel, Confluence, Jenkins, GitHub, Coverity, ClearCase, DOORS, RQM, Cameo, Rhapsody, Oracle, SAP, Microsoft PowerPoint
Senior Principal Quality Engineer – Design Quality & Systems Excellence
Danvers, Massachusetts, United States
$122k-$213k/yrHybridFull Time
Johnson & JohnsonNYSE: JNJ: Develops and manufactures pharmaceutical drugs and medical devices.
12+ YOEBachelor’s in engineering, 12+ years medical device quality engineering experience, expertise in design controls, risk management (ISO 14971), IEC 60601, FMEA, usability (IEC 62366), ISO 13485, and advanced statistical reliability methods.
Senior Principal Quality Engineer – Design Quality & Systems Excellence
Danvers, Massachusetts, United States
$122k-$213k/yrHybridFull Time
Johnson & JohnsonNYSE: JNJ: Global healthcare providing pharmaceuticals and medical technologies.
12+ YOE12+ years in medical device development and quality engineering, Bachelor's/Master's in Engineering, expertise in design controls, risk management (ISO 14971), IEC 60601, FMEA, human factors (IEC 62366), ISO 13485, and advanced statistical/reliability methods.
Analog DevicesNASDAQ: ADI: Designs and manufactures semiconductors for signal processing and power management.
Bachelor's degree in engineering, knowledge of medical device QMS (ISO 13485, FDA, EU MDR), experience with CAPA, audits, document control, training coordination, risk assessment, and proficiency with Microsoft Office and quality management software.
Rochester Electronics: Licensed semiconductor manufacturer and distributor for end-of-life components.
10+ YOE5+ MgmtBachelor's degree in engineering or related field, 10 years quality management experience, 5+ years supervisory experience, semiconductor manufacturing experience, knowledge of ISO9000/IATF16949/AS9100/JEDEC, SPC/LEAN/6 Sigma, auditing and strong computer and communication skills.