Ingeniero De Automatizacion

Cardinal Health

Manufacturing process design and validation
Iso and fda documentation compliance
Root cause analysis for capas
The role involves defining, validating, and documenting manufacturing processes to optimize resources and minimize scrap while ensuring high quality standards

Job Summary

  • The role involves defining, validating, and documenting manufacturing processes to optimize resources and minimize scrap while ensuring high quality standards.
  • Candidates must be responsible for providing technical direction on product design, tooling, and operational requirements in compliance with ISO and FDA regulations.
  • The position requires active participation in EHS initiatives, including stopping unsafe work and collaborating on root cause analysis for incidents.

Matching Summary

The role involves defining, validating, and documenting manufacturing processes to optimize resources and minimize scrap while ensuring high quality standards.

Skills & Requirements

Must-have

  • Manufacturing process design and validation
  • ISO and FDA documentation compliance
  • Root cause analysis for CAPAs
  • PFMEA maintenance and updates
  • Lean Manufacturing and Six Sigma knowledge
  • Minitab and AutoCad proficiency
  • OPEX project planning and execution

Nice-to-have

  • Agile methodology experience
  • BPCS system knowledge
  • Proactive problem solving skills
  • Innovation and continuous improvement mindset
  • Technical training development abilities
  • CAPEX project management experience
  • Adaptability to changing environments

Key Requirements

  • Bachelor's degree in Engineering
  • 2-3 years of similar experience
  • Intermediate to advanced English proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter