Manufacturing Engineer I | Process Validation & Improvement | Changi #HMS

Recruit Express Pte Ltd; Singapore; On-site; SGD 48,000 - 60,000; Full time

Job summary

Recruit Express Pte Ltd seeks a Manufacturing Engineer I to support process qualification, validation and continuous improvement in a regulated medical device manufacturing environment at Changi.

The role involves leading process qualification activities, applying SPC, and driving efficiency with cross-functional teams. This 6-month contract offers potential for permanent placement and responsibilities across quality and engineering disciplines.

Qualifications

• Experience using Statistical Process Control (SPC) and process capability analysis.
• Experience in process qualification, validation and verification in manufacturing.
• Background in regulated medical device environments or similar quality systems.

Responsibilities

• Lead manufacturing process qualification, validation and verification activities.
• Develop and optimise manufacturing processes to improve quality, throughput and cost efficiency.
• Apply SPC and process capability analysis to monitor performance.
• Conduct root cause analysis and implement corrective actions for manufacturing and equipment issues.
• Collaborate with Quality, Supply Chain, R&D, Operations and suppliers on engineering initiatives.
• Support inspection systems, automation and machine vision improvements.
• Prepare and maintain engineering protocols, reports, procedures and technical documentation.
• Drive process standardisation, risk reduction and continuous improvement.

Skills

SPC

Process validation

Continuous improvement

Root cause analysis

Job description

Manufacturing Engineer I | Process Validation & Improvement | Changi

Urgent Hiring – 6-Month Contract to Permanent Opportunity

Location: Changi
Contract: 6 Months, with opportunity to convert to Permanent
Working Arrangement: 5-day work week, office hours

Looking for a Manufacturing Engineer to support process qualification, validation and continuous improvement in a regulated medical device manufacturing environment.

Job Responsibilities

• Lead manufacturing process qualification, validation and verification activities
• Develop and optimise manufacturing processes to improve quality, throughput and cost efficiency
• Apply Statistical Process Control (SPC) and process capability analysis to monitor performance
• Conduct root cause analysis and implement corrective actions for manufacturing and equipment issues
• Collaborate with Quality, Supply Chain, R&D, Operations and suppliers on engineering initiatives
• Support inspection systems, automation and machine vision improvements
• Prepare and maintain engineering protocols, reports, procedures and technical documentation
• Drive process standardisation, risk reduction and continuous improvement