Senior Quality Engineer Clean And Pack , Orthopedics

Johnson & Johnson Innovative Medicine

Raynham, Massachusetts, United States
Base: $79,000.00 - $127,650.00; bonus/equity: not ...
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Global regulations and standards compliance
Non-conformances, capas, customer complaints
Material identification and segregation
** Johnson & Johnson is seeking a Senior Quality Engineer for their Orthopedics division in Raynham, Massachusetts. The role involves ensuring compliance with quality standards, conducting investigations, and collaborating across teams to enhance product quality. **

Job Summary

  • Champions compliance with applicable Global Regulations and standards (e.g. QSRs, ISO, EN and Medical Device Directive (MDD) requirements), including providing support during internal and external audits.
  • Accountability for material identification, material segregation, classification of defect types including the successful application of these techniques on a day-to-day basis in manufacturing.
  • The anticipated base pay range for this position is : $79,000.00 - $127,650.00

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Senior Quality Engineer for their Orthopedics division in Raynham, Massachusetts. The role involves ensuring compliance with quality standards, conducting investigations, and collaborating across teams to enhance product quality. **

Salary

Base: $79,000.00 - $127,650.00; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 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 period10 days Volunteer Leave – 32 hours per calendar year Military Spouse Time-Off – 80 hours per calendar year

Skills & Requirements

Must-have

  • Global Regulations and standards compliance
  • Non-conformances, CAPAs, customer complaints
  • Material identification and segregation
  • Process validation and control
  • Risk management
  • Quality metrics and indicators

Nice-to-have

  • Act with speed, flexibility, and accountability
  • Understand own work impacts enterprise
  • Collaborate effectively with cross-functional teams

Key Requirements

  • Bachelors or equivalent university degree in Engineering or related scientific field
  • 2-4 years of relevant professional work experience
  • Medical Devices industry experience
  • Strong knowledge of quality management systems and regulatory requirements
  • Experience with CAPAs non-conformances, audits, and process validation
  • Strong trending and data analysis skills
  • Troubleshooting expertise

Work Rights

Not specified

Tailored Resume

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