Supplier Quality Engineer Ii

Abiomed

Danvers, Massachusetts, United States of America
Base: $65,000.00 - $104,650.00; bonus/equity: not ...
Not specified (likely onsite given the location context).
Supplier investigations and root-cause analysis
Supplier performance metrics monitoring
Process validation plans
Abiomed, part of Johnson & Johnson MedTech, is seeking a Supplier Quality Engineer II in Danvers, Massachusetts. The role emphasizes supplier quality management for medical devices, requiring a background in electrical engineering and experience in quality assurance

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: 85

Abiomed, part of Johnson & Johnson MedTech, is seeking a Supplier Quality Engineer II in Danvers, Massachusetts. The role emphasizes supplier quality management for medical devices, requiring a background in electrical engineering and experience in quality assurance.

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, including Floating Holidays –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child, Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year, Caregiver Leave – 80 hours in a 52-week rolling period, 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
  • Supplier performance metrics monitoring
  • Process validation plans
  • Technical point of contact with suppliers
  • Resolve quality issues and improve processes

Nice-to-have

  • Patients First culture
  • Innovative product portfolio
  • Dynamic setting
  • Profoundly important work
  • Data Savvy

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

Work Rights

Not specified

Tailored Resume

Cover Letter