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

Recruit Express Pte Ltd; Singapore; On-site; SGD 39,000 - 61,000; Full time

Job summary

Recruit Express Pte Ltd is seeking a Manufacturing Engineer I to support process qualification, validation and continuous improvement in a regulated medical device manufacturing setting at Changi. The role is a 6-month contract with potential conversion to permanent and a 5-day work week in office hours.

The successful candidate will lead qualification/validation activities, optimise processes for quality and throughput, and collaborate across Quality, Supply Chain, R&D and Operations.

Qualifications

• Experience with process qualification and validation in a regulated medical device environment.
• Ability to develop and optimise manufacturing processes for quality and efficiency.
• Familiarity with statistical methods applied to process monitoring.

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.

Skills

Process validation

Continuous improvement

Root cause analysis

Statistical thinking

Tools

SPC

Job description

Manufacturing Engineer I | Process Validation & Improvement | Changi

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