Sr. Design Quality Engineer

Danvers, MA

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Type: Direct Placement

Reference ID: 32037837

Date Posted: 03/23/2026



Apply now: Sr. Design Quality Engineer, location is Hybrid (Danvers, MA). The start date is ASAP for this permanent position.

Job Title: Sr. Design Quality Engineer
Location-Type: Hybrid (Danvers, MA – minimum 3 days onsite)
Start Date Is: ASAP
Duration: Permanent
Compensation Range: $109,000 – $170k (flex, based on experience) 12% bonus (prorated)


Job Description:
Join a leading, innovative MedTech organization in the cardiovascular space, supporting life-saving medical devices used globally. This role offers the opportunity to work on cutting-edge, next-generation products while contributing to both new product development and sustaining efforts in a highly collaborative, fast-paced environment.

This role supports both new product development and sustaining quality efforts for complex cardiovascular medical devices. The ideal candidate is hands-on with design control and risk management, able to actively contribute technically while collaborating across teams.

Day-to-Day Responsibilities:

  • Support design quality activities across new product development and sustaining projects
  • Review and approve design inputs, outputs, and change orders
  • Lead and facilitate risk management activities (ISO 14971, DFMEA/FMEA, hazard analysis)
  • Participate in verification & validation reviews (plans, protocols, reports)
  • Support product cybersecurity risk assessments and planning activities
  • Partner with cross-functional teams (Engineering, R&D, Regulatory, Quality)
  • Support CAPA activities and quality system improvements
  • Assist with audits and ensure compliance with QMS procedures (SOPs)
  • Apply problem-solving methodologies to resolve quality issues

Requirements:

Must-Haves:

  • Bachelor's degree in Engineering or related scientific field
  • 5 years of experience in a highly regulated industry
  • Medical device or biotechnology industry experience
  • Strong knowledge of FDA QSR (21 CFR Part 820) and quality standards (ISO 13485, ISO 14971)
  • Hands-on experience with design control and risk management
  • Experience conducting DFMEA/FMEA and risk management files
  • Strong communication skills and ability to work cross-functionally

Nice-to-Haves:

  • Experience with electromechanical medical devices
  • Familiarity with IEC 62304 and other regulatory standards
  • Experience with cybersecurity risk management in medical devices
  • Knowledge of statistical analysis and reliability tools
  • Advanced degree in engineering or related field

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