Senior / Clinical Innovation Engineer (Innovation Adoption), Medical Technology Office (Contract)

Singapore General Hospital; Singapore; On-site; USD 50,000 - 80,000; Full time

Job summary

A leading hospital seeks an innovation team member to productise selected innovations for operational and clinical adoption. This role involves collaboration with stakeholders, technical support, and adherence to ISO standards within a quality management system, requiring expertise in medical device creation and implementation.

Qualifications

• 2-4 years of relevant working experience in productisation, quality management systems, supply chain or manufacturing.
• Experience in creating medical devices from project to marketed product.
• Familiarity with ISO 13485 and other medical device regulations.

Responsibilities

• Establish processes for productising selected innovations within the SingHealth cluster.
• Interface with end users to gather real-world implementation data.
• Define and maintain processes under an ISO 13485-compliant quality management system.

Skills

Communication

Quality Management Systems

Technical Support

Project Management

Data Analysis

Education

Bachelor’s Degree in Engineering or Science

Master’s Degree or PhD (advantageous)

Job description

As part of the innovation team, your role involves establishing processes and working to productise selected innovations 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 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, Medical Device Regulatory, 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