Mechanical Engineer

Worklane GmbH; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

ResMed is seeking a Mechanical Engineer within the Sleep Product Lifecycle Engineering (PLE) team to own mechanical engineering for released Sleep Care devices and accessories. You will sustain products, drive changes, and collaborate with cross-regional teams to improve performance, reliability, and cost-effectiveness.

The role focuses on maintaining design intent while supporting manufacturing, quality systems, supplier management, and post-market support for global medical devices used by

Qualifications

• Strong mechanical design fundamentals and high-volume manufacturing knowledge.
• Experience with drawings, CAD models, BOMs, and engineering changes.
• Proficiency in 3D CAD modelling (Creo/Pro/Engineer is preferred).
• Ability to investigate issues using structured problem-solving methods.
• Experience working in cross-functional teams in a regulated environment.

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, and manufacturability.
• Develop and maintain CAD drawings, specifications, BOMs, and documentation.
• Perform verification activities for sustaining changes.
• Support CAPA, non-conformance, and product improvements.
• Communicate technical recommendations clearly.

Skills

Mechanical design fundamentals

High-volume manufacturing

Engineering problem solving

Cross-functional collaboration

Documentation and technical writing

Education

Bachelor’s degree in Mechanical Engineering

Tools

Creo

Pro/Engineer

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.

As aMechanical Engineer within the Sleep Product Lifecycle Engineering (PLE) team, you will provide technical ownership and mechanical engineering support for released Sleep Care devices and accessories throughout their lifecycle. The teamis responsible forsustaining products already in market, ensuring they continue to meet quality, reliability, manufacturability, compliance, and customer requirements.

Typical activities include investigating product and manufacturing issues, implementing engineering changes, supporting supplier andcomponentchanges, conducting technical assessments, and driving product improvements. You will work closely with cross-regionalfunctional teams to resolve issues, improve product performance, andmaintainlong-term product continuity.

This role is ideal for engineers who enjoy solving real-world engineering problems, working across multiple disciplines, and delivering practical solutions for products used by millions of patients worldwide.

This role alsoprovidesthe opportunity to become a technical owner of commercially successful medical devices used by millions of patients worldwide. You will gain deepexpertisein product lifecycle management, manufacturing, quality systems, supplier management, and cross-functional engineering leadership.

Team

The Sleep Product Lifecycle Engineering (PLE) teamis responsible forsustaining 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 ismaintainedwhile supporting ongoing manufacturing, quality, supply chain, and business needs. Unlike New Product Development teams, whichfocus on creating and launching new products, the PLE team focuses onmaintainingand 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 andmaintainCAD, 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 Engineeringoran equivalentengineering discipline.

• 3–5+years of relevant mechanical engineering experience, preferablyincluding product sustaining, manufacturing support, productdevelopmentor released-product engineering.

• Strong mechanical designfundamentalsandhigh-volumemanufacturingknowledgeand processes, including part design, tolerance analysis, material selection,injection molding,polymersand design for manufacturability.

• Experience working with engineering drawings, CAD models, specifications, BOMs, engineering changes, and technical documentation.

• Proficiencyin 3D CAD modelling, preferablyCreo / 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 developtechnicallysound 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, alternatecomponentor material qualification, manufacturing transfer, and supply continuity projects.

• Practical understanding of how mechanical design decisions affect manufacturability, reliability, serviceability, cost, quality, and product continuity.