Global Quality & NPI Leader (DFx, ISO 13485)

Celestica

Apodaca

On-site

MXN 1,200,000 - 2,000,000

Full time

2 days ago
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Job summary

Celestica in Mexico is seeking a Senior Quality Manager for New Production Introduction (NPI) focus. You will lead QMS design and deployment, driving DFx and validation strategies to ensure seamless design-to-mass production transitions.

The role oversees regulatory conformance, metrics, and continuous improvement across HealthTech sites. The ideal candidate has 15+ years in quality management with electronics manufacturing, ISO13485 and related standards, and a track record of global QMS

Qualifications

  • Seasoned quality leader with 15+ years in QMS, NPI, and global deployments.
  • Experience in electronic product manufacturing and healthtech environments preferred.
  • Familiarity with ISO13485, FDA/IEC standards and regulatory audits.

Responsibilities

  • Lead QMS design and deployment to meet NPI objectives and customer requirements.
  • Drive DFx reviews and validation strategies from design to mass production.
  • Manage launch readiness, OPS reviews, and customer satisfaction surveys.
  • Ensure regulatory conformance and certifications across sites.
  • Analyze scorecards and audits to identify gaps and drive corrective actions.
  • Own global quality processes and risk mitigation across programs.
  • Educate sites on procedures to sustain long-term quality initiative success.

Skills

Quality Planning
DFx
Launch Readiness
Regulatory Oversight
Quality Analytics
Global QMS
Process Deployment
Training & Capability
Quality Standards
NPI Quality
Validation & DFx
Electronics Manufacturing

Education

Bachelor's degree or higher in Engineering, Quality Management or related field

Tools

ISO 13485
21 CFR 820
ANSI/ISO/ESD

Job description

Celestica in Mexico is seeking a Senior Quality Manager for New Production Introduction (NPI) focus. You will lead QMS design and deployment, driving DFx and validation strategies to ensure seamless design-to-mass production transitions.

The role oversees regulatory conformance, metrics, and continuous improvement across HealthTech sites. The ideal candidate has 15+ years in quality management with electronics manufacturing, ISO13485 and related standards, and a track record of global QMS

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