Lead Scientist, Latex & Chemical Processes

Molnlycke Health Care

Kulim

On-site

MYR 180,000 - 240,000

Full time

5 days ago
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Job summary

Mölnlycke is hiring a Senior Process Scientist for Latex & Chemical Systems at the Malaysia Kulim Hi-Tech Factory. You will lead investigations, develop control strategies, and apply advanced analytics to improve product quality, yield, and manufacturing performance.

The role requires experience with high-volume medical device manufacturing and PFMEA/DOE methodologies. You will collaborate with QA, R&D, Engineering, Maintenance, and suppliers to digitalise processes and protect IP while driving

Qualifications

  • Bachelor’s degree in Chemical/Process/Materials-related field; master’s preferred.
  • Experience with high-volume, regulated manufacturing environments is required or preferred.
  • Strong background in latex/chemical systems and process improvement.

Responsibilities

  • Lead investigations into latex, chemicals, raw materials, and formulations to improve quality and process performance.
  • Develop robust process control strategies, parameter limits, monitoring, escalation, and reaction plans.
  • Apply SPC, MSA, DOE, and capability studies to identify risks and resolve defects.
  • Support PFMEA, control plans, validation, and digitalisation initiatives.
  • Drive improvements in defect reduction, yield, productivity, and material efficiency.
  • Provide technical findings to cross-functional stakeholders and coach teams on data-driven decisions.

Skills

Statistical Process Control
MSA
DOE
Process Capability
PFMEA
Control Plans
8D
Cross-functional troubleshooting
Data-driven decision-making

Education

Bachelor's degree in Chemical Engineering or related field
Master's degree preferred

Tools

SCADA
MES
Data Historian

Job description

Mölnlycke is hiring a Senior Process Scientist for Latex & Chemical Systems at the Malaysia Kulim Hi-Tech Factory. You will lead investigations, develop control strategies, and apply advanced analytics to improve product quality, yield, and manufacturing performance.

The role requires experience with high-volume medical device manufacturing and PFMEA/DOE methodologies. You will collaborate with QA, R&D, Engineering, Maintenance, and suppliers to digitalise processes and protect IP while driving

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