Engineer (Material)

CRAGAR INDUSTRIES PTE LTD; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A medical device manufacturing company in Singapore is seeking an experienced Engineer (Material) to manage and optimize material-related processes. This role involves ensuring the quality and compliance of raw materials used in production, collaborating with cross-functional teams in procurement and logistics. The ideal candidate has at least 5 years of experience in material engineering and a strong understanding of regulatory standards like ISO 13485. Excellent communication and analytical skills are essential for this position.

Qualifications

• Minimum 5 years of experience in material engineering or mechanical engineering.
• Experience in a MedTech or regulated manufacturing environment.
• Familiarity with HS code classification and international shipping.

Responsibilities

• Manage and optimize material-related processes for medical device production.
• Develop material specifications in compliance with ISO 13485.
• Oversee procurement and inspection of raw materials.
• Support Supply Chain Management on Vendor Managed Inventory.
• Liaise with vendors on material-related tooling.

Skills

Knowledge of material properties

Procurement systems experience

Inspection protocols

Supply chain coordination

Excellent communication skills

Problem-solving abilities

Education

Diploma or bachelor’s degree in Materials Science or Engineering

Job description

Job Summary

The Engineer (Material) will be responsible for managing and optimizing material-related processes within Cragar Industries. This role ensures the quality, availability, and compliance of raw materials used in medical device production, while supporting cross-functional teams in procurement, inspection, logistics, and engineering coordination.

Key Responsibilities

Core Material Engineering Duties

• Evaluate and select appropriate materials for medical device components based on drawings requirement, regulatory, and cost criteria.
• Develop and maintain material specifications and documentation in compliance with ISO 13485 regulatory requirements.
• Conduct failure analysis and root cause investigations related to material issues.
• Collaborate with R&D and manufacturing teams to support new product development and process improvements.

Procurement & Inspection

• Oversee procurement of raw materials for medical device component production, ensuring timely availability and cost-effectiveness.
• Manage incoming inspection of all raw materials to ensure conformance to specifications and regulatory standards.

Supply Chain & Logistics Support

• Support Supply Chain Management (SCM) in coordinating with customers on Vendor Managed Inventory (VMI) and Third-Party Logistics (3PL) matters.
• Assist in all shipment-related activities, e.g. declaration of HS codes for customer deliveries.

Vendor & Engineering Collaboration

• Liaise with vendors and suppliers regarding fixtures, gauges, and other material-related tooling.
• Support Engineering and Quality Control (QC) teams in all matters related to Request for Quotation (RFQ) processes.

Job Requirements

Education & Experience

• Diploma or bachelor’s degree in Materials Science, Engineering, or related field.
• Minimum 5 years of experience in material engineering or mechanical engineering, preferably in a MedTech or regulated manufacturing environment.

Technical Skills

• Strong knowledge of material properties, testing methods, and regulatory standards (e.g., ISO 13485, FDA).
• Experience with procurement systems, inspection protocols, and supply chain coordination.
• Familiarity with HS code classification and international shipping documentation.

Soft Skills

• Excellent communication and coordination skills across cross-functional teams.
• Strong analytical and problem-solving abilities.
• Detail-oriented with a commitment to quality and compliance.