Lead Process Validation Engineer (6M Contract, Changi)

Recruit Express Pte Ltd; Singapore; On-site; SGD 67,000 - 89,000; Full time

Job summary

Recruit Express Pte Ltd in Singapore is seeking a qualified engineer to lead manufacturing process qualification and validation activities at the Changi site. The role focuses on improving production processes, quality and efficiency, and supports automation and inspection systems.

Requirements include a Bachelor's in Engineering and hands-on experience with SPC, process capability analysis, and regulated manufacturing environments; medical device exposure is a plus.

Qualifications

• Experience in manufacturing process validation, qualification or verification.
• Knowledge of Statistical Process Control (SPC) and process capability analysis.
• Experience in manufacturing process improvement and troubleshooting.
• Familiar with manufacturing quality systems and regulatory requirements.
• Medical device or regulated manufacturing experience is an advantage.

Responsibilities

• Lead manufacturing process qualification and validation activities.
• Improve production processes, quality and efficiency.
• Analyse manufacturing data using SPC and statistical methods.
• Investigate process issues and implement corrective actions.
• Support automation, inspection systems and manufacturing improvements.
• Prepare engineering documentation, validation protocols and reports.

Skills

SPC and process capability analysis

Manufacturing process improvement

Troubleshooting

Regulatory quality systems

Medical device or regulated env

Education

Bachelor's Degree in Engineering

Job description

Recruit Express Pte Ltd in Singapore is seeking a qualified engineer to lead manufacturing process qualification and validation activities at the Changi site. The role focuses on improving production processes, quality and efficiency, and supports automation and inspection systems.

Requirements include a Bachelor's in Engineering and hands-on experience with SPC, process capability analysis, and regulated manufacturing environments; medical device exposure is a plus.