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Morgan Advanced Materials

Co-designs and manufactures mission-critical material solutions

Quality Engineer

Quality EngineeringConfirmed live in the last 24 hours
Full-timeNew Bedford, MA, USA$74.5k - $111.7kIn-person

About the Job

Requirements

  • A bachelor's degree in Engineering from an accredited college or university is required; Mechanical, Electrical, or Chemical Engineering is preferred.
  • At least two years of work experience in a manufacturing environment is required; experience in aerospace or medical manufacturing is preferred.
  • ASQ Certified Quality Engineer (CQE) certification is desirable but not required.
  • The role requires eligibility to access Controlled Unclassified Information subject to ITAR, EAR, and NRC regulations. The individual must be a United States citizen, permanent resident alien, or protected individual as defined by 8 U.S.C. 1324b(a)(3) and 22 CFR 120.15.
  • The candidate must have quality orientation and high attention to detail.
  • The candidate must have experience working with high-performance teams.
  • The candidate must have problem-analysis and problem-resolution skills.
  • The candidate must be familiar with Microsoft Word and Excel.
  • The candidate must be able to clearly present ideas and reports in written and verbal formats.
  • The candidate must be able to work well with subordinates, peers, and superiors in all company departments, and with external company contacts.
  • The candidate must have time-management, planning, and negotiation skills.

Responsibilities

  • Update documentation, train personnel, and implement quality processes such as material review board (MRB), return material authorization (RMA), corrective and preventive action (CAPA), and nonconformance material report (NCMR) processes.
  • Direct MRB activities, including facilitating MRB meetings, tracking nonconformances, and analyzing NCMRs and RMAs.
  • Conduct analytical investigations and determine root causes for nonconformances and deviations identified through scrap analysis, NCMRs, and RMAs.
  • Maintain the CAPA database.
  • Coordinate the RMA process, including approval, verification upon receipt, disposition, and issuance of subsequent CAPAs; respond to customer-related supplier corrective action requests (SCARs) as required.
  • Issue, monitor, and evaluate CAPAs for effectiveness and timeliness.
  • Create or process engineering change orders (ECOs), process routers, drawings, and other written documentation in accordance with quality-system requirements.
  • Monitor supplier performance through scorecards or grading, analyze receiving inspection (RI) measurement data using statistical quality control (SQC), track NCMRs, and conduct supplier audits and visits as required.
  • Maintain the internal auditing program to sustain certification to ISO standards and ensure system effectiveness.
  • Conduct internal, third-party, and customer audits, including internal quality audits against ISO 9001, ISO 14001, AS 9100, and ISO 13485.
  • Analyze data and generate reports from enterprise resource planning (ERP) data using Minitab and Microsoft Excel.
  • Create validation protocols (IQ, OQ, and PQ), execute the protocols, and document reports when required; assist with design of experiments (DOE), analysis of variance (ANOVA), and other analytical methods to optimize processes.
  • Develop, document, and train inspectors using internal procedures and geometric dimensioning and tolerancing (GD&T) guidelines; design or specify gauging and test equipment for inspectors.
  • Implement and maintain statistical process control (SPC) and SQC using Infinity QS.
  • Develop quality plans, preliminary and full failure mode and effects analyses (pFMEAs and FMEAs) for new and existing products, and assist with control plans and other documentation during new product development.
  • Conduct capability studies and variation-reduction activities to improve processes.
  • Compile and write training materials and conduct training sessions on quality tools and techniques.
  • Create or update RI and final-product manufacturing inspection record (MIR) cards for product inspection and testing.
  • Set up, program, and operate coordinate measuring machines (CMMs), SmartScope, and other measurement and inspection tools; improve measurement techniques and detection methods using gauge repeatability and reproducibility (GRR), measurement system analyses (MSAs), and poka-yoke.
  • Communicate with production associates to understand issues and concerns and implement countermeasures.
  • Research and propose documentation, training, and inspection methods, including electronic record retention, automated visual inspection, and inspector certification programs.
  • Perform other tasks as requested by the supervisor.
  • Perform tasks safely and efficiently in compliance with local, state, and federal environmental, health, and safety regulations and company EHS guidelines, including required training and proper personal protective equipment; report hazardous conditions and work-related injuries or illnesses to the supervisor.
  • Perform other job-related duties and follow job-related instructions from an authorized company representative.

Desired Qualifications

  • Knowledge of SolidWorks or AutoCAD is preferred.
  • ASQ Certified Quality Engineer (CQE) certification is desirable but not required.
  • Experience in aerospace or medical manufacturing is preferred.

About the Company

Morgan Advanced Materials

Co-designs and manufactures mission-critical material solutions

Morgan Advanced Materials designs and manufactures mission-critical materials and components by combining material science, deep application expertise, and precise manufacturing processes. Their products support essential systems that help people move, build, and thrive, and they aim to power human progress where it matters most. The company co-designs solutions with customers, focusing on performance and reliability for demanding environments. Unlike others who only supply materials, Morgan emphasizes an integrated approach—bridging science, engineering, and manufacturing to tailor solutions that meet specific applications. The strategic goal is to become the leading force in their chosen markets, driven by operational excellence, efficient asset use, and maximizing the value of their portfolio.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Windsor, United Kingdom
Founded
1856

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