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Astrix Technology

Quality Engineer (Medical Device)

Career Insights for Product Quality Engineer

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What they do

A Product Quality Engineer evaluates and tests products and manufacturing systems, to ensure that products are produced that meet quality and performance standards as well as safety and regulatory requirements. Develops product quality standards and monitors production and product testing.

$95,435 / year median in New Jersey

+3% projected growth

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Job Description

  • Quality Engineer (Medical Device)
  • Quality Assurance Rahway, New Jersey, NONE + Added - 15/07/2026
Pay Rate Low:
90000 |
Pay Rate High:
100000 Our client, a global leader in the medical device industry, is looking for a experienced Quality Engineer to join their growing team. This is a great opportunity to work with a company that provides specialty medical technology solutions for some of the worlds most complex medical devices. +
  • Schedule
  • : Onsite ~8a-5p M-F +
  • Salary
  • : $90-100K + 5% annual bonus eligibility +
  • Type
  • : Direct Hire +
  • Location:
  • Union County, NJ
  • Position Summary
  • The Quality Engineer is responsible for supporting product and process quality by developing inspection methods, investigating quality issues, and driving continuous improvement initiatives. This role partners closely with Manufacturing and Engineering to ensure compliance with customer, regulatory, and quality system requirements.
  • Key Responsibilities
  • + Develop and implement inspection, testing, and quality evaluation methods for products and manufacturing processes.
+ Perform quality assurance testing and analyze results using statistical quality tools. + Investigate nonconforming products, customer complaints, and quality issues using Root Cause Analysis and support CAPA activities. + Create inspection plans, automated measurement programs, and maintain quality documentation. + Collaborate with Manufacturing and Engineering to resolve day-to-day quality concerns and drive process improvements. + Support and maintain the Quality Management System (QMS) in compliance with ISO 13485 and applicable regulatory requirements. + Manage multiple quality projects and perform other duties as assigned.
  • Required Qualifications
  • + Bachelor's degree in Engineering or a related technical field.
+ 2-4 years of Quality Engineering experience in medical device (preferred) or pharmaceutical manufacturing. + Experience working within an
ISO 13485
Quality Management System. + Proficiency with quality tools, including SPC, Gage R&R, and Process Capability. + Experience conducting Root Cause Analysis and supporting CAPA investigations. + Ability to read and interpret engineering drawings and dimensional measurement requirements. + Strong analytical, problem-solving, organizational, and communication skills. _This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_ _INDBH_ _\#LI-KM1_We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.