Senior Quality Engineer Clean And Pack , Orthopedics

J&J FAMILY OF COMPANIES

Raynham, Massachusetts, United States of America
Base: $79,000.00 - $127,650.00; bonus/equity: not ...
Not specified
Quality management systems knowledge
Regulatory compliance expertise
Process validation and control
Johnson & Johnson is seeking a Senior Quality Engineer Clean and Pack for their Orthopedics division in Raynham, Massachusetts. The ideal candidate will have experience in the medical devices industry, particularly in quality management and regulatory compliance

Job Summary

  • Johnson & Johnson is recruiting for a Senior Quality Engineer Clean and Pack to join our exceptional team in Raynham, MA.
  • This role champions compliance with applicable global regulations and standards, supports audits, and leads quality investigations and validations.
  • Employees are eligible for comprehensive benefits including retirement plans, vacation, sick time, parental leave, and volunteer leave.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Quality Engineer Clean and Pack for their Orthopedics division in Raynham, Massachusetts. The ideal candidate will have experience in the medical devices industry, particularly in quality management and regulatory compliance.

Salary

Base: $79,000.00 - $127,650.00; Bonus/Equity: Not specified; Benefits: Retirement plans, vacation, sick time, parental leave, volunteer leave

Skills & Requirements

Must-have

  • Quality management systems knowledge
  • Regulatory compliance expertise
  • Process validation and control
  • CAPA and non-conformance management
  • Root cause investigation skills
  • Data analysis and trending
  • Audit support and compliance

Nice-to-have

  • Process Excellence / Six Sigma certification
  • Cross-functional team collaboration
  • Strong communication skills
  • Problem-solving and analytical skills
  • Leadership in quality standards
  • Flexibility and accountability

Key Requirements

  • Bachelor's degree in Engineering or related field
  • 2-4 years medical device industry experience
  • Knowledge of ISO 13485 and FDA QSR
  • Experience with CAPAs and audits
  • Process validation experience
  • Ability to travel up to 10%

Work Rights

Not specified

Tailored Resume

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