System Engineer (Medical Device/ West/ 1 YEAR contract)

GMP TECHNOLOGIES (S) PTE LTD| Date Posted: 26-Nov-2020
EA Licence No: 09C3051|EA Personal Registration No: R1330693
Save Job
Job Nature:
Position Level:
Bachelor's / Honours

Job Description


  • Develop product engineering requirements and guiding architectural design to ensure that products meet customer and business expectations for safety, regulatory, quality, performance, functionality, reliability and efficacy.
  • Involves defining processes for technical platforms, system requirements, input/output and working parameters for hardware and/or software compatibility.
  • Systems Engineering conceives system interfaces within the device and considers implications with interfacing to business applications. This includes identifying, analyzing and resolving system design weaknesses.
  • Build productive internal/external working relationships to ensure that the system objectives are balanced with overall project objectives.
  • Define design structure to provide desired functionality per product and user requirements and Medical Device Regulatory (MDR) Standards for applicable regions.
  • Identify, define and communicate compliance requirements for all aspects of projects. Develop measures, feedback and reporting mechanisms for Senior Management.
  • Occasionally leads the work of project teams and might formally train junior members.
  • Manage and contribute to new/existing projects and provide advice/direction in primary areas of expertise where possible.
  • Leveraging professional expertise and relationships to contribute to drive business strategy and results


  • Bachelor degree in Engineering
  • A minimum of 1 to 3 years of product design or engineering experience in product development environment.
  • Preferably with basic knowledge in medical device regulations for US FDA, EU MDD/MDR.
  • Formal training in project management, experiment methodology, Six Sigma, DFSS, or other related engineering topics will be added advantageous.
  • Demonstrates good knowledge of regulations and customer specifications and their impact on design parameters (i.e. marketing, clinical, regulatory, manufacturing, quality, IP).
  • Candidate must be willing to commit the full 1-year contract duration.

To apply, please visit to and search for Job Code: 17130.

To find out more about this opportunity, please contact Lionel Liew at [Click Here to Email Your Resume].


We regret that only shortlisted candidates will be notified.


GMP Technologies (S) Pte Ltd   |   EA Licence: 11C3793 |   EA Personnel: Lionel Liew   |   Registration No: R1330693

Company Overview