Singapore Health Services Pte Ltd

Clinical Innovation Engineer, Medical Technology Office

Job Category:  Administration
Posting Date:  18-Mar-2023

Job Description

You will assist in the identification, validation and selection of unmet clinical needs, as well as participate in solution generation and prototyping. You will conduct testing, create supporting documentation required for patenting and regulatory approval, as well as work with partners on commercialisation strategy.


You will coordinate and compile relevant information for grants and other funding applications, as well as manage and drive project tasks to ensure timely completion of project milestones. You will ensure proper documentation for meetings, follow-up processes and recommendations for further action.


You will support the device development team in brainstorming, technical design, administrative tasks and procurement. You will also support the management of medical technology innovation grants, such as the grant application process as well as grant award and progress reporting. You will also support the department in joint education initiatives to nurture and develop Clinician Innovators.


You will ensure compliance with regulatory requirements and organisation’s policies, and support record-keeping and documentation needed for compliance.

Job Requirements

  • Master’s or Bachelor’s Degree in Biochemistry, Chemistry, Chemical Engineering, Biomedical Engineering, Biotechnology, Information Technology, Computing or Software Engineering
  • Prior experience in the following areas will be an advantage: medical technology innovation leading to the development of concept ideas into products, in-vitro or in-vivo diagnostics or assay development for mobile platforms, and application development and/or deployment
  • Excellent people management and communication skills
  • Excellent problem solving skills with strong focus in technical writing
  • Strong knowledge in IT, CAD and Simulation Skills, e.g. LabView, MatLab, SolidWorks, AutoCad
  • Good knowledge in ISO 13485, ISO14155, Good Clinical Practice (GCP), Regulatory Affairs, Medical Device Standards, Intellectual Property Strategy will be an advantage
  • Knowledge of trial procedures, institutional, Centralised Institutional Review Board and regulatory authority (HSA) requirements will be an advantage
  • Meticulous, responsible, self-motivated and able to work within tight timelines
  • Must be fully vaccinated against COVID-19