R&D Engineer – Medical Device NPD & Cross-Functional Lead

Biosensors Interventional Technologies Pte Ltd; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

Biosensors Interventional Technologies Pte Ltd in Singapore is seeking an engineer to drive new product development from concept through verification and transfer to manufacturing.

The role requires 2–4 years in a regulated setting, strong design and process development skills, and ability to work with cross-functional teams including regulatory aspects.

You will collaborate on lab work, document technical reports, and support cross-functional teams to ensure compliant medical device development.

Qualifications

• Minimum Degree in Mechanical/Material/Chemical/Bio-Engineering or relevant.

Responsibilities

• To lead or support the full new product development project lifecycles from concept stage to verification and validation and to manufacturing transfer and product launch.
• To support, coordinate, and execute in continuous improvements projects, cost-down projects, and sustaining activities.
• To lead or actively participate in R&D projects and act as the technical lead for cross-functional teams
• Provide guidance to junior engineers and technicians, and assist in lab management
• To execute in all required technical documentation works.
• To participate and contribute to cross-functional team activities

Skills

Product design

Process development

Medical device design

Regulatory affairs

Analytical skills

Team collaboration

Technical documentation

Lab management

Education

Bachelor's degree in Mechanical/Material/Chemical/Bio-Engineering

Job description

Biosensors Interventional Technologies Pte Ltd in Singapore is seeking an engineer to drive new product development from concept through verification and transfer to manufacturing.

The role requires 2–4 years in a regulated setting, strong design and process development skills, and ability to work with cross-functional teams including regulatory aspects.

You will collaborate on lab work, document technical reports, and support cross-functional teams to ensure compliant medical device development.