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Submitted by melvin@sginnov… on Thu, 10/23/2025 - 16:32
Designation
Medical Device Development Associate
Description

About Biobot Surgical

Biobot Surgical is the first surgical robotics venture to emerge from Singapore’s dynamic academic and clinical ecosystem.

 

Key Responsibilities

As a Medical Device Development Associate, you will gain hands-on experience across engineering, quality, regulatory, and product functions in a MedTech startup. You will rotate through     Product / Engineering, Regulatory Affairs, Quality Assurance & Quality Control, Clinical / Voice-of-Customer (VoC) & Trial Support. You will be empowered to own tasks across the product lifecycle and shadow senior staff (CTO, Engineering & Product Managers).

 

Rotation Tracks & Key Responsibilities

1. Product / Engineering

  • Translate user (clinical) feedback into engineering & usability requirements
  • Participate in design reviews, prototyping and verification & validation testing, troubleshooting variance and deep dive into solution
  • Work with mechanical/electrical/firmware teams to understand system integration
  • Contribute to technical documentation
  • Ensure traceability under design control standards

2. Regulatory Affairs

  • Learn how regulatory requirements relate to product documentation
  • Assist in preparing regulatory submissions
  • Support in bridging engineering and regulatory perspectives for compliance

3. Clinical / User-Voice & Trial Support

  • Lead Voice-of-Customer (VoC) interviews/surveys with clinicians, nurses and users
  • Assist trial planning (protocol input, site engagement) — lighter execution support
  • Observe clinical workflows, collect user feedback to feed into product design

4. Shadowing & Strategic Exposure

  • Shadow the CTO, Engineering Leads, Product Manager in decision-making, planning, project reviews
  • Attend cross-functional meetings to see how engineering, clinical, regulatory, and business functions integrate
  • Contribute to special projects (e.g. technology reviews, product roadmap alignment, risk assessments)

 

Qualifications and Competencies

  • Master’s or Ph.D. in Engineering (Biomedical, Mechanical, Electrical, or related) or equivalent technical discipline
  • Strong aptitude for testing, analysis, problem-solving and system thinking
  • Experience (academic or lab) in device design, prototyping, testing or instrumentation
  • Good communication skills and ability to engage with users/clinicians
  • Excellent technical writing skills.
  • Flexible, curious, and able to adapt across domains
  • Some exposure to regulated environments is a plus
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