Sr. Manufacturing Engineer

Medtronic UK

Kulim, Malaysia
**
Support sustaining manufacturing line
Process optimization and investigations
Root cause analysis and corrective actions
** Medtronic is seeking a Sr. Manufacturing Engineer to support high-scale production in their Kulim, Malaysia facility. The role involves optimizing manufacturing processes, ensuring compliance with regulatory requirements, and collaborating with various teams to enhance production efficiency. **

Job Summary

  • You will support processes as required to provide daily operations support to the manufacturing floor including inputs to monitoring and control to maintain robust processes.
  • Investigate and resolve equipment, process, and product non-conformances through root cause analysis and corrective actions.
  • Medtronic offers a competitive Salary and flexible Benefits Package.

Matching Summary

Match Score: 75

** Medtronic is seeking a Sr. Manufacturing Engineer to support high-scale production in their Kulim, Malaysia facility. The role involves optimizing manufacturing processes, ensuring compliance with regulatory requirements, and collaborating with various teams to enhance production efficiency. **

Skills & Requirements

Must-have

  • Support sustaining manufacturing line
  • Process optimization and investigations
  • Root cause analysis and corrective actions
  • Design and optimize manufacturing processes
  • Compliance with regulatory requirements
  • Statistical process control techniques

Nice-to-have

  • Champion healthcare access and equity
  • Break down barriers to innovation
  • Disciplined and well-resourced innovation
  • Deep commitment to quality, ethics, and patients

Key Requirements

  • Bachelor's degree in engineering or sciences with 4+ years of experience
  • Master's degree in engineering or sciences with 2+ years of experience
  • Strong understanding of Master Validation
  • Knowledge of GD&T & experience in interpreting mechanical drawings
  • Experience with risk management (pFMEA, dFMEA)
  • Experience in FDA 21 CFR Part 820 Medical Device Manufacturing, or ISO 13485 is preferred
  • Knowledge of Engineering Change management processes and PLM tools

Work Rights

Not specified

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