Senior / Clinical Innovation Engineer (Innovation Adoption), MTO (Contract)

Singapore Health Services Pte Ltd (SingHealth HQ); Singapore; On-site; SGD 65,000 - 90,000; Full time

Job summary

A leading healthcare organization in Singapore is seeking an innovation team member to develop and implement processes for productising selected innovations, collaborating with stakeholders and providing technical support. The ideal candidate will have a strong background in engineering, quality management, and medical device development, aiming to enhance clinical practices and operational efficiencies.

Qualifications

• 2-4 years of relevant working experience in productisation and quality management systems.
• Experience in implementing and maintaining quality management system.
• Familiarity with ISO 13485 and regulatory standards for medical devices.

Responsibilities

• Establish processes to productise innovations for operational and clinical settings.
• Gather real-world implementation and clinical data to assess innovations' impact.
• Define and maintain ISO 13485-compliant quality management processes.

Skills

Communication

Project Management

Quality Management

Education

Bachelor’s Degree in Engineering or Science

Master’s Degree or PhD

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