Biomedical Engineer

Parailabs; Singapore; On-site; SGD 80,000 - 120,000; Full time

Job summary

SME Careers in Singapore seeks a Biomedical Engineer to evaluate and refine AI models on biomedical topics, ensuring technical correctness and safe guidance. You will challenge language models with domain-specific tasks, review prompts and responses, and provide structured feedback to improve model performance while upholding biomedical ethics and regulatory considerations.

Applicants should have a strong background in biomechanics, biomaterials, bioinstrumentation, or related areas, plus

Qualifications

• 4+ years of professional biomedical engineering experience.
• Bachelor’s degree in Biomedical Engineering required; Master’s/PhD or advanced credentials strongly preferred.
• Experience with AI data training, annotation, red‑teaming, or evaluating AI-generated technical content is a strong plus.
• Familiarity with ISO 13485, IEC 60601, ISO 14971, FDA design controls (21 CFR 820), verification & validation, risk management, biocompatibility concepts (ISO 10993) is a plus.

Responsibilities

• Evaluate AI-generated responses for technical accuracy, logical soundness, completeness, and clarity across biomedical engineering topics.
• Challenge advanced language models with realistic biomedical engineering scenarios, calculations, and design/analysis reasoning tasks.
• Review and refine AI-generated prompts, model responses, explanations, and step-by-step solutions (including unit handling and correct interpretation of constraints).
• Provide structured feedback that identifies factual errors, unsafe recommendations, unsupported clinical claims, missing assumptions, invalid simplifications, misuse of standards, or incomplete reasoning.
• Assess model performance on topics such as: Biomechanics, Bioinstrumentation & sensors, Biomedical signals, Medical device design, Biomaterials, Imaging & measurement, Verification/validation & risk
• Help shape AI communication standards for biomedical content, including how models explain assumptions, risk/limitations, what must be verified experimentally, and when to elevate to clinical/regulatory experts.
• Ensure AI-generated content reflects responsible biomedical engineering practice—especially around patient safety, clinical claims, and regulatory-sensitive topics.

Skills

Biomechanics

Bioinstrumentation

Biomedical signals

Biomaterials

Medical device design

Imaging & measurement

Verification/validation

Risk management

AI data training

Education

Bachelor’s degree in Biomedical Engineering

Job description

If you are a biomedical engineer who thrives on technical precision, applied problem-solving, and rigorous engineering reasoning in health and life-science contexts, this is a unique opportunity to contribute directly to how the next generation of AI systems understand and communicate complex biomedical engineering concepts. We are looking for biomedical engineering specialists who can evaluate, challenge, and refine advanced language models on domain-specific topics. Your expertise as a Biomedical Engineer will directly help improve the world’s premier AI models—and play an important role in shaping the future of AI. This role is with SME Careers, a fast-growing AI Data Services company and subsidiary of SuperAnnotate, delivering training data for many of the world’s largest AI companies and foundation-model labs.

Important: There is no immediate project for this role; however, if qualified, you will be among the first experts we reach out to when relevant opportunities arise. This will also provide you with access to future projects available through our expert network.

Responsibilities

• Evaluate AI-generated responses for technical accuracy, logical soundness, completeness, and clarity across biomedical engineering topics.
• Challenge advanced language models with realistic biomedical engineering scenarios, calculations, and design/analysis reasoning tasks.
• Review and refine AI-generated prompts, model responses, explanations, and step-by-step solutions (including unit handling and correct interpretation of constraints).
• Provide structured feedback that identifies factual errors, unsafe recommendations, unsupported clinical claims, missing assumptions, invalid simplifications, misuse of standards, or incomplete reasoning.
• Assess model performance on topics such as: Biomechanics, Bioinstrumentation & sensors, Biomedical signals, Medical device design, Biomaterials, Imaging & measurement, Verification/validation & risk
• Help shape AI communication standards for biomedical content, including how models explain assumptions, risk/limitations, what must be verified experimentally, and when to elevate to clinical/regulatory experts.
• Ensure AI-generated content reflects responsible biomedical engineering practice—especially around patient safety, clinical claims, and regulatory-sensitive topics.

Requirements

• 4+ years of professional biomedical engineering experience, with significant hands‑on work in one or more areas such as medical devices, biomechanics, biomaterials, tissue engineering, bioinstrumentation, imaging systems, signals & systems (physiologic), rehabilitation engineering, clinical engineering, quality/regulatory, manufacturing/validation, or a closely related specialty.
• Deep knowledge of biomedical engineering fundamentals, such as physiology for engineers, transport phenomena in biological systems, biomechanics, materials behavior in biological environments, biosignals, sensor/measurement systems, and systems modeling (depending on specialty).
• Strong comfort with technical assumptions, constraints, unit consistency, and defensible reasoning (including limitations, uncertainty, and safety considerations).
• Bachelor’s degree in Biomedical Engineering (or closely related) required; Master’s/PhD or advanced credentials strongly preferred.
• Experience with AI data training, annotation, red‑teaming, or evaluating AI-generated technical content is a strong plus.
• Familiarity with any of the following is a plus (not required): ISO 13485, IEC 60601, ISO 14971, FDA design controls (21 CFR 820), verification & validation, risk management, biocompatibility concepts (ISO 10993), or clinical workflow constraints.

Eligible countries: Bangladesh, Bhutan, Brazil, Cambodia, Germany, India, Indonesia, Malaysia, Nepal, Pakistan, Singapore, Sri Lanka, Thailand, The Philippines, The United States, Timor Leste, Vietnam

Skills

Medical Device Design Biomechanics Biomaterials Tissue Engineering Bioinstrumentation