Supplier Quality Engineer Ii

Abiomed

Danvers, Massachusetts, United States of America
Base: $65,000.00 - $104,650.00; bonus/equity: not ...
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Supplier investigations and root-cause analysis
Monitor supplier performance metrics
Assess risk through fmeas
** Abiomed, part of Johnson & Johnson MedTech, is seeking a Supplier Quality Engineer II in Danvers, Massachusetts. The role focuses on ensuring supplier quality for electronic components while promoting a patient-centered culture and innovation in medical device technology. **

Job Summary

  • This role involves hands-on project management, collaboration with multi-functional teams, and ensuring that supplier qualification processes align with quality standards and company objectives.
  • The Supplier Quality Engineer II is responsible for cross-functional Quality Assurance, Quality Management/Compliance and activities associated with all Abiomed products and processes with a focus on supplier for the Danvers plant.
  • The anticipated base pay range for this position is : $65,000.00 - $104,650.00

Matching Summary

Match Score: 75

** Abiomed, part of Johnson & Johnson MedTech, is seeking a Supplier Quality Engineer II in Danvers, Massachusetts. The role focuses on ensuring supplier quality for electronic components while promoting a patient-centered culture and innovation in medical device technology. **

Salary

Base: $65,000.00 - $104,650.00; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year, Sick time - 40 hours per calendar year, Holiday pay –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours, Bereavement Leave – 240 hours for an immediate family member, Caregiver Leave – 80 hours, Volunteer Leave – 32 hours per calendar year, Military Spouse Time-Off – 80 hours per calendar year

Skills & Requirements

Must-have

  • Supplier investigations and root-cause analysis
  • Monitor supplier performance metrics
  • Assess risk through FMEAs
  • Process validation plans
  • Resolve quality issues and improve processes

Nice-to-have

  • Patients First! culture
  • Innovative product portfolio
  • Dynamic setting enables positive people

Key Requirements

  • BS degree in electrical engineering or related engineering field
  • 2+ years of related experience
  • Experience in the medical device industry is strongly preferred
  • Knowledge of cGMP, FDA 820 QSR, ISO 13485
  • Knowledge of statistics
  • Six Sigma, Lean Certifications

Work Rights

Not specified

Tailored Resume

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