Supplier Quality Engineer Ii

Abiomed

Danvers, Massachusetts, United States of America
Base: $65,000.00 - $104,650.00; bonus/equity: elig...
Not specified (assumed to be onsite based on location)
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 to join their team in Danvers, Massachusetts. The role focuses on supplier quality assurance and compliance for medical devices, emphasizing collaboration with suppliers and internal teams

Job Summary

  • 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.
  • 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 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 to join their team in Danvers, Massachusetts. The role focuses on supplier quality assurance and compliance for medical devices, emphasizing collaboration with suppliers and internal teams.

Salary

Base: $65,000.00 - $104,650.00; Bonus/Equity: Eligible for long-term incentive program; Benefits: Vacation, Sick time, Holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off

Skills & Requirements

Must-have

  • Supplier investigations and root-cause analysis
  • Monitor supplier performance metrics
  • Assess risk through FMEAs
  • Technical partner with internal inspection teams
  • Resolve quality issues and improve processes

Nice-to-have

  • Patients First! culture
  • Innovative product portfolio
  • Profoundly impact health for humanity
  • Inclusive work environment
  • 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 (hypothesis testing, capability analysis, DOE, MSA)

Work Rights

Not specified

Tailored Resume

Cover Letter