Mechanical Engineer

ResMed (Malaysia) Sdn Bhd (MY); Singapore; On-site; SGD 90,000 - 120,000; Full time

Job summary

ResMed is seeking a Mechanical Engineer to join the Sleep Product Lifecycle Engineering (PLE) team. You will sustain and improve released Sleep Care products, lead or support changes, and collaborate across engineering, manufacturing, quality, regulatory and supplier teams globally.

The role emphasizes design for manufacturability, CAD work, documentation, verification, and driving reliability and cost improvements while maintaining compliance with medical device standards.

Qualifications

• Bachelor's degree in Mechanical Engineering or equivalent.
• 3–5+ years in mechanical engineering, preferably in product sustaining/manufacturing support.
• Strong mechanical design fundamentals and knowledge of high-volume manufacturing.
• Experience with engineering drawings, CAD models, specs, BOMs and engineering changes.
• Proficiency in 3D CAD modelling, preferably Creo/Pro/E.
• Ability to perform structured problem-solving and impact assessments.
• Excellent written and verbal communication; able to document decisions clearly.
• Ability to work in cross-functional teams and manage multiple priorities.

Responsibilities

• Support released Sleep Care products throughout their lifecycle.
• Lead or support product, supplier, material, and manufacturing changes.
• Investigate product, manufacturing, supplier, and field issues.
• Assess engineering changes for quality, reliability, manufacturability and compliance.
• Develop and maintain CAD drawings, specifications, BOMs, and engineering documentation.
• Perform verification activities for sustaining changes.
• Support CAPA, non-conformance, and product improvement activities.
• Collaborate with cross-functional teams and suppliers.
• Drive reliability, manufacturability, and cost improvements.
• Clearly communicate technical recommendations and decisions.

Skills

Mechanical design fundamentals

3D CAD modelling

Creo / Pro Engineer

Product sustaining / PLM

Cross-functional teamwork

Problem solving

Documentation & specs

Manufacturing support

Communication skills

Verification & validation

Education

Bachelor's degree in Mechanical Engineering

Tools

Creo

Job description

Job Summary

Imagine working with a global team of talented people who are committed to creating the world’s best medical technology. Imagine a role where your skills and attributes contribute to improving millions of lives. Because at ResMed, you will.

Team

The Sleep Product Lifecycle Engineering (PLE) team is responsible for sustaining and improving released Sleep Care products throughout their lifecycle. The team owns engineering activities related to product changes, supplier and material changes, manufacturing support, quality investigations, reliability improvements, and product continuity initiatives.

Mechanical Engineers within PLE serve as technical owners of released products, ensuring design intent is maintained while supporting ongoing manufacturing, quality, supply chain, and business needs. Unlike New Product Development teams that focus on creating and launching new products, the PLE team focuses on maintaining and improving products already released to market.

To deliver these outcomes, PLE engineers collaborate closely with Electrical, Systems, Manufacturing, Quality, Regulatory, Supplier Quality, Product Management, and Operations teams across ResMed's global organization.

Responsibilities

• Support released Sleep Care products throughout their lifecycle.
• Lead or support product, supplier, material, and manufacturing changes.
• Investigate product, manufacturing, supplier, and field issues.
• Assess engineering changes for impact to quality, reliability, manufacturability, and compliance.
• Develop and maintain CAD, drawings, specifications, BOMs, and engineering documentation.
• Perform verification activities for sustaining changes.
• Support CAPA, non-conformance, and product improvement activities.
• Collaborate with cross-functional teams and suppliers.
• Drive reliability, manufacturability, and cost improvements.
• Clearly communicate technical recommendations and decisions.

Requirements

The ideal candidate will have a strong mechanical engineering foundation, practical problem-solving ability, and experience supporting products in a manufacturing or regulated environment.

Required qualifications and experience:

• Bachelor’s degree in Mechanical Engineering or an equivalent engineering discipline.
• 3–5+ years of relevant mechanical engineering experience, preferably including product sustaining, manufacturing support, product development or released-product engineering.
• Strong mechanical design fundamentals and high-volume manufacturing knowledge and processes, including part design, tolerance analysis, material selection, injection molding, polymers and design for manufacturability.
• Experience working with engineering drawings, CAD models, specifications, BOMs, engineering changes, and technical documentation.
• Proficiency in 3D CAD modelling, preferably Creo / Pro Engineer or equivalent CAD software.
• Ability to investigate technical issues using logical, structured, and methodical problem‑solving methods.
• Ability to perform engineering impact assessments and develop technically sound recommendations based on available evidence.
• Strong written and verbal communication skills, with the ability to document technical decisions clearly and concisely.
• Ability to work effectively in cross-functional teams and manage multiple priorities in a dynamic environment.

Preferred Experience

Preferred qualifications and experience:

• Experience in the medical device industry or another regulated industry.
• Experience supporting released products in a Product Lifecycle Engineering, sustaining engineering, manufacturing engineering, quality engineering, or product support environment.
• Familiarity with engineering change control, design controls, risk management, verification and validation, and post‑market product support.
• Understanding of quality management systems and applicable standards, includingISO 13485, ISO 14971, and Good Documentation Practices (GDP).
• Experience supporting internal, supplier, customer, or regulatory audits.
• Experience with supplier change qualification, alternate component or material qualification, manufacturing transfer, and supply continuity projects.
• Practical understanding of how mechanical design decisions affect manufacturability, reliability, serviceability, cost, quality, and product continuity.

Company Culture

Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates.