Manager, Supplier Quality- Shockwave Medical

Johnson & Johnson Innovative Medicine

Santa Clara, California, United States of America
Base: $118,000.00 - $203,550.00; bonus/equity: not...
Supplier quality management
Quality system compliance
Risk management program
The Manager of Supplier Quality is responsible for the administration, supervision, and development of the Supplier Quality group, providing leadership for the organization’s quality engineering, quality system, and risk management program

Job Summary

  • The Manager of Supplier Quality is responsible for the administration, supervision, and development of the Supplier Quality group, providing leadership for the organization’s quality engineering, quality system, and risk management program.
  • This role defines processes and systems, and implements procedures to ensure compliance with applicable regulatory standards such as ISO 13485, ISO 14971, 21 CFR Part 820, and EU MDR.
  • Essential job functions include supplier management, defining quality requirements for manufacturing line transfers, supporting manufacturing operations, and managing and developing the Supplier Quality Engineers team.

Matching Summary

The Manager of Supplier Quality is responsible for the administration, supervision, and development of the Supplier Quality group, providing leadership for the organization’s quality engineering, quality system, and risk management program.

Salary

Base: $118,000.00 - $203,550.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Supplier Quality Management
  • Quality System Compliance
  • Risk Management Program
  • ISO 13485 Compliance
  • 21 CFR Part 820 Compliance
  • EU MDR Compliance

Nice-to-have

  • Process Improvement Collaboration
  • Cross-functional Team Leadership
  • Regulatory Change Monitoring
  • Johnson & Johnson Credo Integration

Key Requirements

  • BS degree in engineering discipline and 10+ years of experience
  • MS degree in engineering discipline and 8+ years of experience
  • 2+ years of experience managing others
  • Strong understanding of cGMP, FDA 820 QSR, ISO 13485
  • Ability to travel up to 25%

Work Rights

Not specified

Tailored Resume

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