Mechanical Engineer (Medical Devices)

Location: Singapore, Singapore

Company

hirify.global develops medical technology and Sleep Care devices designed to improve the health and quality of life of millions of patients.

What you will do

• Provide technical ownership and mechanical engineering support for released Sleep Care products and accessories throughout their lifecycle.
• Lead or support product, supplier, material, and manufacturing changes.
• Investigate product, manufacturing, supplier, and field issues and develop evidence-based technical recommendations.
• Assess engineering changes for quality, reliability, manufacturability, compliance, cost, and product continuity impacts.
• Maintain CAD models, drawings, specifications, BOMs, and engineering documentation, and perform verification activities for sustaining changes.
• Collaborate with Electrical, Systems, Manufacturing, Quality, Regulatory, Supplier Quality, Product Management, Operations teams, and suppliers.

Requirements

• Bachelor’s degree in Mechanical Engineering or an equivalent engineering discipline.
• 3–5+ years of relevant mechanical engineering experience, preferably in product sustaining, manufacturing support, product development, or released-product engineering.
• Strong mechanical design fundamentals and knowledge of high-volume manufacturing, part design, tolerance analysis, material selection, injection molding, polymers, and design for manufacturability.
• Experience with engineering drawings, CAD models, specifications, BOMs, engineering changes, and technical documentation.
• Proficiency in 3D CAD modeling, preferably Creo/Pro Engineer or equivalent software.
• Structured technical problem-solving, impact assessment, clear communication, cross-functional collaboration, and the ability to manage multiple priorities.

Nice to have

• Experience in medical devices or another regulated industry.
• Experience with Product Lifecycle Engineering, sustaining engineering, manufacturing engineering, quality engineering, or product support.
• Familiarity with engineering change control, design controls, risk management, verification and validation, and post-market product support.
• Knowledge of quality management systems and standards including ISO 13485, ISO 14971, and Good Documentation Practices.
• Experience with supplier change qualification, alternate component or material qualification, manufacturing transfer, supply continuity projects, or technical audits.

Culture & Benefits

• Work in a global, cross-functional environment supporting products used by millions of patients worldwide.
• Culture focused on excellence, innovation, diversity, inclusion, and individual expression.
• Opportunity to develop deep expertise in product lifecycle management, manufacturing, quality systems, supplier management, and engineering leadership.
• Work on practical engineering improvements for commercially successful medical devices.