Engineer II (ME)

Sanmina; Singapore; On-site; SGD 60,000 - 100,000; Full time

Job summary

Sanmina Corporation in Singapore seeks an Engineer II (ME) to configure and deploy MES (42Q) settings, troubleshoot MES uptime, and maintain validation documentation. You will collaborate cross-functionally to improve manufacturing processes on PCBA/SMT/Box Build lines.

The role requires a degree or diploma in engineering, strong data-analysis skills, and familiarity with ISO 13485 and ERP/MES integrations.

Qualifications

• Bachelor's degree or Diploma in engineering (Industrial, Manufacturing, Computer Science or related field).
• Experience in PCBA/SMT/Box Build manufacturing with MES implementation.
• Proficient in MS Office/ Google Suite applications.
• Proficiency in data analysis and reporting.
• Strong understanding of manufacturing processes and principles.
• Knowledge of industrial automation and control systems.
• Strong communication and interpersonal skills.
• Familiarity with medical device manufacturing standards (ISO 13485) and software validation practices is highly preferred.
• Basic understanding of system integrations (e.g., ERP to MES) is an advantage.

Responsibilities

• Configure and deploy MES settings to meet product-specific manufacturing requirements and liaison with development teams.
• Maintain and troubleshoot MES systems for uptime and reliability.
• Maintain SFDC configurations and Medical Validation documents.
• Collaborate to identify process improvements using MES functionalities.
• Maintain SOPs for the MES system and document changes.
• Analyze production data to identify trends, yield, and improvement areas.
• Train and mentor junior staff and participate in continuous improvement initiatives.
• Stand-in for team members as needed.

Skills

Data analysis

Manufacturing processes

Communication skills

Interpersonal skills

Problem solving

Education

Bachelor's degree in engineering

Diploma in engineering

Tools

42Q MES

MS Office / Google Suite

ERP–MES integration basics

Software validation practices

Job description

Description

Sanmina Corporation (Nasdaq: SANM) is a global powerhouse in integrated manufacturing solutions serving the fastest growing segments of the global Electronics Manufacturing Services (EMS) market. We are a global engine providing the end-to-end manufacturing backbone for the world's most essential and innovative brands. Whether it's autonomous vehicles, life-saving medical tech, next-gen aerospace, or AI/cloud infrastructure - our integrated solutions don’t just meet standards—they redefine them. Engineer II (ME) Job Responsibilities

• Configure and deploy 42Q MES settings to meet product-specific manufacturing requirements on the shop floor, and serve as the primary liaison to provide feedback and escalated requirements to the Corporate 42Q Development Team
• Maintain and troubleshoot existing (42Q) MES systems to ensure optimal performance and uptime.
• Maintain the accuracy and reliability of all SFDC configurations and Medical Validation documents.
• Collaborate with teams to identify and implement process improvements using MES functionalities.
• Maintain the standard operating procedures (SOPs) for the MES system.
• Resolve Line system issues in a timely manner.
• Analyze production data from the MES system to identify trends, yield, and areas for improvement.
• Train& mentor new or junior staffs.
• Participate in continuous improvement initiatives.
• Stand-in for team members whenever the need arises.
• Other duties as assigned by the Supervisor or Management. Job Requirements
• Bachelor's degree or Diploma in engineering(Industrial, Manufacturing, Computer Science or related field).
• Experience in the PCBA/SMT/Box Build manufacturing industry, with dedicated experience in MES implementation.
• Experience in PCBA/SMT/Box build manufacturing industry is preferred.
• Proficient in MS Office/ Google Suite applications.
• Proficiency in data analysis and reporting.
• Strong understanding of manufacturing processes and principles.
• Knowledge of industrial automation and control systems.
• Strong communication and interpersonal skills.
• Familiarity with medical device manufacturing standards (e.g., ISO 13485) and software validation practices is highly preferred.
• Basic understanding of system integrations (e.g., ERP to MES, equipment API integration) is an advantage.