You will be responsible for the design, prototyping, testing mechanical systems for medical devices, and assisting the Office of Innovation fulfil its objectives of coordinating and managing innovation initiatives under CGH. You will assist the Manager/Senior Manager to oversee the innovation projects under Office of Innovation and manage engagements with relevant stakeholders. The job functions include but not limited to :
Responsibilities
Product Development
- Support product ideation and design conceptualisation, including preparing design requirements, design intent, market analysis, and feature comparisons.
- Develop detailed designs using computer-aided tools in mechanical, electrical, and firmware domains.
- Build and refine prototypes using 3D printing or by coordinating with external partners.
- Conduct design verification, including DFMEA, test plan preparation and design testing.
- Manage the use and upkeep of prototyping facilities, including 3D printers, materials, and related equipment.
- Prepare documentation (design briefs, PowerPoint) to engage internal and external stakeholders.
- Prepare design brief to engage with internal & external stakeholders.
- Coordinate end-to-end project from scoping of project, budgeting, preparing funding application, preparing approval papers, coordination with funders/sponsors, and project closure.
Project Management
Coordinate end-to-end project from scoping of project, budgeting, preparing funding application, preparing approval papers, coordination with funders/sponsors, and project closure.
General Duties
- Foster effective working relationships with internal stakeholders and assist the operational and clinical champions in their innovation ideas and projects.
- Contribute technical inputs when engaging with external funding bodies, IHLs, SMEs, and companies for co-development of innovation projects.
- Promote innovation culture within CGH and beyond by organising workshops, events and forums to raise awareness of Office of Innovation.
- Any other duties assigned from time to time.
Requirements
- Bachelor’s Degree in Mechanical Engineering, Bioengineering, Biomedical Engineering, or a related field from a recognised university.
- Those with lesser years of experience, but with strong projects portfolio, are encouraged to apply. Entry level graduates are welcome to apply.
- Experience in the following functions is a must: (1) Product Development; (2) Project Management.
- Experience in mechanical design and prototyping, including proficiency in CAD software (e.g., SolidWorks).
- Experiences in additive manufacturing (e.g. resin and filament 3D printing), plastics design, and lightweight mechanisms are highly valued.
- Experiences operating, optimising, and maintaining 3D printers, including slicer software, print setup, troubleshooting, and post‑processing, is an advantage.
- Experiences selecting and integrating electronics components (e.g., motors and actuators) or simple mechanisms for test rigs, jigs, and fixtures.
- Knowledge of testing and validation processes for mechanical systems, including test plan development, execution, and documentation.
- Knowledge of relevant regulatory standards and requirements such as ISO 13485 and FDA regulations for medical devices is an advantage.
- Proficiency in Microsoft Office applications (Word, Excel, PowerPoint) for reporting and documentation.
- Good interpersonal & communication skills
- Strong teamwork and ability to manage cross‑functional and institutional relationships
Only shortlisted candidates will be notified.