Manufacturing Engineer 1

Jabil Circuit (Singapore) Pte Ltd; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A prominent manufacturing company in Singapore is looking for a Manufacturing Engineer I to support the engineering department in processes related to medical devices. The role involves ensuring compliance with ISO 13485, supporting manufacturing workflows, and driving continuous improvements. Ideal candidates should have a diploma in Mechanical or Mechatronic Engineering and at least 2 years of relevant experience in a regulated environment. Strong problem-solving and communication skills are essential for this position. The company offers a dynamic work environment focused on quality and safety.

Qualifications

• Minimum 2 years of experience in manufacturing engineering.
• Experience in a medical device or regulated manufacturing environment is preferred.

Responsibilities

• Support daily manufacturing operations for medical devices.
• Ensure compliance with ISO 13485 and GMP.
• Drive continuous improvement and cost reduction initiatives.

Skills

Mechanical Engineering

Mechatronic Engineering

Analytical skills

Problem-solving

Effective communication

Education

Diploma in Mechanical Engineering or related discipline

Tools

Engineering tools

Job description

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.

The Manufacturing Engineer I supports the Engineering Department in the planning, design, implementation, validation, and continuous improvement of manufacturing processes for medical devices. This role ensures that production systems comply with applicable regulatory and quality management system (QMS) requirements, while achieving targets for performance, reliability, safety, cost, and delivery.

The position focuses on analyzing manufacturing workflows, optimizing processes, and supporting compliant production operations in accordance with ISO 13485, internal procedures, and applicable regulatory standards.

Key Responsibilities

Manufacturing & Process Support

• Support daily manufacturing operations to ensure compliant, efficient, and consistent production of medical devices.
• Develop, document, and maintain assembly processes, work instructions, and standard operating procedures (SOPs).
• Perform and support high-level assembly (HLA) activities by interpreting engineering drawings, specifications, and procedures.
• Train production operators on approved processes, equipment usage, and GMP requirements.

Validation & Regulatory Compliance

• Support medical device process and equipment validation activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Ensure manufacturing processes comply with ISO 13485, Good Manufacturing Practices (GMP), and internal QMS requirements.
<>Participate in change control activities to ensure regulated changes are reviewed, approved, and documented prior to implementation.

Quality & Continuous Improvement

• Support New Product Introduction (NPI) builds and process transfers in accordance with regulatory and quality requirements.
• Investigate product and process quality issues, perform root cause analysis, and implement Root Cause and Corrective Action (RCCA/CAPA).
• Assist in product evaluation, process characterization, and data collection for quality and regulatory purposes.
• Drive continuous improvement and cost reduction initiatives while maintaining regulatory compliance and product quality.

Equipment & Production Line Support

• Support preventive maintenance (PM) activities and maintain records for engineering tools, fixtures, and production equipment.
• Assist with production line reconfiguration and machine/workstation moves, including equipment installation, setup, and qualification.
• Ensure equipment and tooling are suitable for validated and controlled manufacturing environments.

Safety & Compliance

• Adhere to all safety, health, environmental, and company security policies.
• Ensure compliance with documentation, data integrity, and record retention requirements.
• Maintain effective communication with cross-functional teams including Quality, Manufacturing, and Engineering.

Required Qualifications & Experience

• Diploma, Advanced/Higher/Graduate Diploma, or equivalent in Mechanical Engineering, Mechatronic Engineering, or a related discipline.
• Minimum 2 years of experience in manufacturing engineering, preferably within a medical device or regulated manufacturing environment.

Preferred Knowledge & Skills

• Knowledge of medical device manufacturing regulations and standards, including ISO 13485.
• Hands‑on experience supporting IQ, OQ, PQ, and validation documentation.
• Familiarity with GMP, risk management, and change control processes.
• Strong analytical, problem‑solving, and documentation skills.
• Effective written and verbal communication skills.

Accessibility Accommodation

Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.