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Quality Assurance Engineer (Watertown)
Quality Assurance Engineer (Watertown)EPS Connects LLC • Watertown, CT, United States
Quality Assurance Engineer (Watertown)

Quality Assurance Engineer (Watertown)

EPS Connects LLC • Watertown, CT, United States
11 days ago
Job type
  • Full-time
Job description

Quality Assurance Engineer Medical Device Manufacturing (Onsite | Watertown, CT)

Are you ready to take on a hands-on quality leadership role in a highly regulated, fast-paced manufacturing environment? Were looking for a Quality Assurance Engineer to join a global medical device manufacturer known for technical excellence, precision manufacturing, and continuous innovation.

This role offers the opportunity to play a key part in ensuring compliance, quality, and safety across multiple programs supporting advanced medical and life science technologies. If you thrive in an environment where engineering rigor meets real-world impact this could be the next step in your career.

What Youll Do

  • Drive compliance and quality excellence : Ensure all processes meet FDA (21 CFR Part 820), ISO 13485, and global regulatory standards.
  • Be audit-ready at all times : Support internal and external audits, ensuring full compliance and documentation integrity.
  • Lead risk and failure analysis : Conduct risk assessments, FMEA, and implement effective CAPA strategies to improve process robustness and patient safety.
  • Partner across disciplines : Collaborate closely with R&D, Manufacturing, and Regulatory Affairs to ensure quality is built into every stage of product development and production.
  • Champion documentation and testing rigor : Develop, execute, and validate test protocols, maintaining thorough records and applying sound statistical analysis.
  • Train and influence : Share best practices, conduct quality and compliance training, and build a culture of continuous improvement.

What You Bring

  • Bachelors degree in Engineering, Life Sciences, or related field .
  • 3+ years of experience in a regulated manufacturing environment (medical device preferred).
  • Deep understanding of FDA, ISO 13485, and 21 CFR Part 820 standards.
  • Hands-on experience with root cause analysis, CAPA, FMEA, validation, and data-driven problem-solving .
  • Proficiency with tools such as Minitab, Excel, Power BI, SolidWorks, or ERP / QMS platforms .
  • Professional certifications such as CQE, Six Sigma, or ISO 13485 Lead Auditor are highly valued.

    • Why Youll Love It

  • A culture that values technical excellence, precision, and problem-solving .
  • The opportunity to work with cutting-edge medical technologies that directly improve lives.
  • A mix of hands-on work and strategic quality leadership ideal for someone who wants both responsibility and visibility.
  • Competitive compensation, strong mentorship, and the chance to grow within a leading medical manufacturing organization.
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    Quality Assurance Engineer • Watertown, CT, United States