Principal / Engineer, Innovation (Innovation Adoption), Medical Technology Office (Contract)

Singapore National Eye Centre; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading medical technology office in Singapore seeks a Principal / Engineer for Innovation Adoption. Responsibilities include productising medical innovations and collaborating with stakeholders to implement solutions. Candidates should have a relevant Bachelor's degree and 2-4 years of relevant experience, with familiarity in quality management systems and medical device regulations.

Qualifications

• 2-4 years of relevant working experience in productisation or quality management systems.
• Experience in creating medical devices from project to marketed product.
• Familiarity with ISO 13485, ISO 14971, IEC 62304, and Medical Device Regulations.

Responsibilities

• Establish processes to productise medical devices and AI innovations.
• Gather real-world implementation and cost-effectiveness data.
• Maintain ISO 13485-compliant quality management system.

Skills

Productisation

Quality management systems

Excellent communication skills

Technical support

Education

Bachelor’s Degree in Engineering or Science

Master’s Degree or PhD

Job description

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Principal / Engineer, Innovation (Innovation Adoption), Medical Technology Office (Contract)

Job Category: Administration

Posting Date: 26 Jul 2025

As part of the innovation team, your role involves establishing processes and working to productise selected innovations including medical devices, software and AI medical devices for adoption within the SingHealth cluster. This includes collaborating with internal stakeholders and external manufacturing partners to implement these innovations in operational and clinical settings, while providing post-deployment technical support.

A key aspect of the role involves interfacing with end users and stakeholders to gather real-world implementation, clinical and cost-effectiveness data. This data supports impact assessment of adopted innovations and their eventual commercial potential. Additionally, the role encompasses defining, implementing and maintaining relevant processes and procedures under the office's ISO 13485-compliant quality management system.

Job Requirements

• Bachelor’s Degree in Engineering or Science
• 2-4 years of relevant working experience in productisation, quality management systems, supply chain, enterprise IT and/or manufacturing
• A Master’s Degree or PhD is advantageous
• Experience in creating medical devices from project to marketed product
• Experience in implementation/maintenance of a quality management system
• Familiarity with ISO 13485, ISO 14971, IEC 62304, AI Medical Devices, Software-as-Medical-Device (SAMD), Medical Device Regulations, Medical Device Standards, Risk Management for Medical Devices
• Knowledge of business or financing models for medical technology industries
• Meticulous, responsible and self-motivated individual with excellent communication skills