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Quality Engineer

Job in South Plainfield, Middlesex County, New Jersey, 07080, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-03-03
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering, Biomedical Engineer
Job Description & How to Apply Below

Summary:
We are seeking a Quality Engineer with experience in the medical device industry to support quality assurance, regulatory compliance, and continuous improvement initiatives. The ideal candidate will have a strong background in FDA regulations, ISO 13485, risk management (ISO 14971), and product lifecycle management, including design control and CAPA systems.

Roles & Responsibilities:

  • Ensure compliance with FDA 21 CFR Part 820, ISO 13485, and other applicable regulatory standards.
  • Support design control activities including design verification/validation, risk analysis (FMEA, FTA), and product release.
  • Develop and maintain quality documentation, including SOPs, work instructions, inspection plans, and validation protocols.
  • Perform root cause investigations and drive Corrective and Preventive Actions (CAPA) to resolution.
  • Conduct or support internal audits, supplier audits, and regulatory inspections.
  • Monitor and improve product quality metrics (yield, complaints, non-conformances, etc.).
  • Collaborate with cross-functional teams (R&D, Manufacturing, Regulatory, Supply Chain) to ensure quality is built into processes and products.
  • Lead or assist in supplier quality management activities, including qualifications, audits, and performance monitoring.
  • Participate in risk management processes and ensure appropriate risk controls are implemented.
  • Support change control processes for product or process changes.
  • Contribute to continuous improvement initiatives using tools such as Six Sigma, Lean, and 8D.
Education & Experience :
  • Bachelor's degree in Engineering, Life Sciences, or related field.
  • 2–5+ years of quality engineering experience in the medical device or regulated industry.
  • Strong knowledge of FDA QSR (21 CFR Part 820) and ISO 13485.
  • Experience with risk management (ISO 14971) and design control practices.
  • Hands-on experience with CAPA, Company, validations (IQ/OQ/PQ), and audits.
  • Proficient in quality tools such as FMEA, 8D, Root Cause Analysis, etc.
  • Excellent analytical, documentation, and communication skills.
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