29 Clinical Diagnostics jobs in Singapore

We are seeking a skilled and motivated Bioinformatics Scientist to support the development of next-generation diagnostic products and contribute to data analytics in Software as a Medical Device (SaMD) applications. This role offers the opportunity to work on cutting-edge bioinformatics pipelines and multi-omics data analysis, collaborating with cross-functional teams and external partners to bring innovative diagnostics to market.

• Design, develop, and deploy bioinformatics pipelines for in-vitro diagnostics (IVD), including NGS data processing and reporting.
• Support multi-omics data analysis for biomarker discovery and diagnostics assay development.
• Provide bioinformatics and biostatistical analysis for clinical studies and product validation.
• Collaborate with software engineers and product teams to integrate analytics into SaMD platforms.
• Contribute to the development of predictive models using machine learning and statistical approaches.
• Ensure reproducibility, scalability, and regulatory compliance of bioinformatics workflows.
• Document pipeline architecture, analysis protocols, and validation results.

• PhD or Bachelor's/Master's degree in Bioinformatics, Computational Biology, or a related field.
• 2 -3 years of industry experience in bioinformatics or clinical diagnostics.
• Proficiency in Python, R, or MATLAB; experience with workflow tools like Nextflow, Snakemake, or CWL.
• Familiarity with biostatistics and machine learning for biological data analysis.
• Experience with tools such as Biopython, Bioconductor, and cloud-based deployment environments.
• Knowledge of statistical software (e.g., R, SAS, SPSS, Minitab) is a plus.
• Exposure to IVD product development and regulatory standards is advantageous.
• Strong communication skills and ability to work independently and in cross-disciplinary teams.

Interested candidates who wish to apply for the advertised position, please click on "Apply". We regret that only shortlisted candidates will be notified.

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Overview

The Medical Affairs team collaborates with the leaders of Sleep, Respiratory Care, SaaS, ResMed Healthcare, and Asia Growth Markets to ensure our work, especially our clinical research and market access projects, align with their strategic priorities. We also review key government policies, as part of the continuous evaluation and improvement process that helps us maintain global compliance across an ever-shifting landscape of legal and regulatory requirements. The two, research and compliance, work hand-in-hand, and when balanced properly allow us to generate important clinical, economic and market evidence, that improves the lives of patients in ways that are scientifically valid, clinically relevant and ethically sound.

• Let’s talk about the team: The primary role of Clinical Science & Innovation function is to develop new product concepts, prototypes and technologies, that are aligned to ResMed's strategy. Key deliverables include developing business cases with strategic focus and commercial value that enables a global view of clinical science and deep technology as it pertains to ResMed's world.

We are seeking an enthusiastic and detail-oriented Clinical Development Specialist – Diagnostics to join our Medical Affairs team. In this role, you will play a critical part in the design, implementation, and oversight of clinical development activities that support our sleep diagnostics portfolio. You’ll work cross-functionally to ensure that our products have the correct requirements and to define and execute on strategies to generate high-quality evidence to support the safe and effective use of diagnostic solutions across various healthcare settings.

This is a unique opportunity to contribute to the development of cutting-edge diagnostics that enable timely, accurate decision-making for patients and providers.

• Support the planning and execution of clinical studies—including analytical validation, clinical validation, and usability studies—aligned with diagnostic development goals.
• Assist in developing study protocols, investigator brochures, case report forms (CRFs), and other clinical study documents.
• Collaborate with internal stakeholders such as Regulatory Affairs, Clinical Operations, R&D, and Marketing to ensure integrated study planning and execution.
• Liaise with external investigators, clinical sites, and contract research organizations (CROs) to support effective study conduct and data integrity.
• Participate in data analysis and interpretation activities to support product development, regulatory submissions, and scientific communications.
• Track study timelines, milestones, and budgets to ensure clinical projects are completed on time and within scope.
• Maintain a strong understanding of diagnostic regulatory pathways (e.g., FDA, CE-IVD, CLIA) and ensure compliance with applicable clinical and ethical guidelines.
• Contribute to the development of abstracts, posters, and manuscripts to communicate clinical evidence to external audiences.

• Bachelor’s degree in life sciences, biomedical engineering, public health, or a related field.
• 3+ years of experience in clinical development or clinical research, with a focus on diagnostics, in vitro diagnostics (IVDs), or medical devices.
• Familiarity with clinical validation and usability studies for diagnostics.
• Working knowledge of Good Clinical Practice (GCP), ISO 14155, and diagnostic regulatory frameworks.
• Strong organizational skills and the ability to manage multiple projects simultaneously.
• Excellent verbal and written communication skills.
• Highly skilled in stakeholder management across different regions and time-zones.

• Advanced degree (e.g., MS, PhD, MPH)
• Experience supporting regulatory submissions for diagnostic products (e.g., 510(k), PMA, IVDR)
• Prior work in a Medical Affairs or translational science environment
• Experience with diagnostic studies in sleep disorders and respiratory care

• Scientific and Technical Expertise
• Project Management
• Diagnostic Regulatory Knowledge
• Cross-functional Collaboration
• Strategic Thinking
• Communication and Presentation
• Quality and Compliance Focus

Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now! We commit to respond to every applicant.

• Mid-Senior level

• Full-time

• Health Care Provider

• Software Development, IT Services and IT Consulting, and Medical Equipment Manufacturing

Referrals increase your chances of interviewing at Resmed by 2x

Queenstown, Central Singapore Community Development Council, Singapore 4 months ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Overview
The Medical Affairs team collaborates with the leaders of Sleep, Respiratory Care, SaaS, ResMed Healthcare, and Asia Growth Markets to ensure our work, especially our clinical research and market access projects, align with their strategic priorities. We also review key government policies, as part of the continuous evaluation and improvement process that helps us maintain global compliance across an ever-shifting landscape of legal and regulatory requirements. The two, research and compliance, work hand-in-hand, and when balanced properly allow us to generate important clinical, economic and market evidence, that improves the lives of patients in ways that are scientifically valid, clinically relevant and ethically sound.
Let’s talk about the team:
The primary role of Clinical Science & Innovation function is to develop new product concepts, prototypes and technologies, that are aligned to ResMed's strategy. Key deliverables include developing business cases with strategic focus and commercial value that enables a global view of clinical science and deep technology as it pertains to ResMed's world.
Role
We are seeking an enthusiastic and detail-oriented
Clinical Development Specialist – Diagnostics
to join our Medical Affairs team. In this role, you will play a critical part in the design, implementation, and oversight of clinical development activities that support our sleep diagnostics portfolio. You’ll work cross-functionally to ensure that our products have the correct requirements and to define and execute on strategies to generate high-quality evidence to support the safe and effective use of diagnostic solutions across various healthcare settings.
This is a unique opportunity to contribute to the development of cutting-edge diagnostics that enable timely, accurate decision-making for patients and providers.
Key Responsibilities
Support the planning and execution of clinical studies—including analytical validation, clinical validation, and usability studies—aligned with diagnostic development goals.
Assist in developing study protocols, investigator brochures, case report forms (CRFs), and other clinical study documents.
Collaborate with internal stakeholders such as Regulatory Affairs, Clinical Operations, R&D, and Marketing to ensure integrated study planning and execution.
Liaise with external investigators, clinical sites, and contract research organizations (CROs) to support effective study conduct and data integrity.
Participate in data analysis and interpretation activities to support product development, regulatory submissions, and scientific communications.
Track study timelines, milestones, and budgets to ensure clinical projects are completed on time and within scope.
Maintain a strong understanding of diagnostic regulatory pathways (e.g., FDA, CE-IVD, CLIA) and ensure compliance with applicable clinical and ethical guidelines.
Contribute to the development of abstracts, posters, and manuscripts to communicate clinical evidence to external audiences.
Let’s talk about you
Required
Bachelor’s degree in life sciences, biomedical engineering, public health, or a related field.
3+ years of experience in clinical development or clinical research, with a focus on diagnostics, in vitro diagnostics (IVDs), or medical devices.
Familiarity with clinical validation and usability studies for diagnostics.
Working knowledge of Good Clinical Practice (GCP), ISO 14155, and diagnostic regulatory frameworks.
Strong organizational skills and the ability to manage multiple projects simultaneously.
Excellent verbal and written communication skills.
Highly skilled in stakeholder management across different regions and time-zones.
Preferred
Advanced degree (e.g., MS, PhD, MPH)
Experience supporting regulatory submissions for diagnostic products (e.g., 510(k), PMA, IVDR)
Prior work in a Medical Affairs or translational science environment
Experience with diagnostic studies in sleep disorders and respiratory care
Core Competencies
Scientific and Technical Expertise
Project Management
Diagnostic Regulatory Knowledge
Cross-functional Collaboration
Strategic Thinking
Communication and Presentation
Quality and Compliance Focus
Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now! We commit to respond to every applicant.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Health Care Provider
Industries
Software Development, IT Services and IT Consulting, and Medical Equipment Manufacturing
Referrals increase your chances of interviewing at Resmed by 2x
Queenstown, Central Singapore Community Development Council, Singapore 4 months ago
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Job Title: Respiratory Laboratory Assistant

As a Respiratory Laboratory Assistant, you will play a crucial role in delivering high-quality patient care in our laboratory. We are seeking a skilled professional who can provide specialized services in accordance with established hospital policies and procedures.

As a seasoned Medical Technology Project Manager, you will be responsible for the end-to-end planning and execution of cross-functional projects within the medical sector. These may include new product development, manufacturing transfers, or market launches.

The ideal candidate will have a proven track record of delivering projects on time, within scope, and budget while maintaining compliance with internal quality systems and regulatory requirements.

• Lead cross-functional teams to deliver new medical devices from concept to commercialization.
• Develop and manage detailed project plans, timelines, budgets, and risk registers.
• Navigate organizational change and evolution, embedding new operating models.

You will work closely with internal and external stakeholders to define project scope, goals, and deliverables. The ability to communicate effectively and facilitate regular project meetings is essential.

As a Project Manager, you will ensure all project documentation is completed accurately and on time. You will also monitor production and supply chain performance, implementing corrective actions as needed.

• Sustainability
• Leadership
• Risk Management
• Inventory Control
• Operational Excellence
• Project Management

We are looking for a highly motivated and organized individual who can drive project velocity, ensuring successful initial implementation of projects into production.

Experience in leveraging technology to drive data-based decisions and automation across the business is highly desirable.

The Project Lead oversees the entire lifecycle of medical technology projects, from concept to commercialization.

o Develop and manage comprehensive project plans, timelines, and budgets.

o Drive execution through all phases of the product development lifecycle (PDP/NPD), including design.

The Project Lead must possess excellent leadership skills, business acumen, and the ability to motivate and direct cross-functional teams towards a common goal. They should have a strong understanding of medical device regulations, quality systems, and industry best practices.

o Deliver high-quality medical devices that meet customer needs and exceed expectations.

The Project Leader is responsible for end-to-end planning, execution and delivery of projects across various functions within the medical technology sector. These may include new product development, internal business-driven manufacturing development, clinical studies, regulatory submissions, manufacturing transfers or market launches. The Project Leader ensures all project objectives are met on time, within scope and budget while maintaining compliance with internal quality systems and regulatory requirements.

• Lead cross-functional teams to deliver new medical devices from concept to commercialization.
• Develop and manage detailed project plans, timelines, budgets and project trackers.
• Drive execution through all phases of the product development lifecycle.
• Ensure compliance with ISO 13485, FDA QSR and other relevant standards/regulations.

• Project management skills.
• Leadership and team management skills.
• Communication and stakeholder management skills.
• Risk management and mitigation skills.
• Documentation and reporting skills.

This role offers opportunities for professional growth and development in a dynamic and innovative environment.

• Bachelor's degree in Business Administration, Engineering or related field.
• 5+ years of experience in project management or related field.
• Proven track record of delivering projects on time and within budget.

Job Highlight:

• Kaki Bukit
• Basic up to $2,500
• Work Hours: (Mon – Fri)
• Morning Shift: 7:00 AM – 3:00 PM
• Afternoon Shift: 3:00 PM – 11:00 PM
  (Monday – Friday)
• Allowances: Transport Allowance: $10/month, Shift Allowance (Afternoon Shift): 180/month

Responsibilities

• Perform production processes independently following work instructions, process descriptions, cGMP, and safety guidelines.
• Operate equipment and carry out assigned process steps within the production cell.
• Maintain a safe and clean work environment in line with 5S principles.
• Participate in continuous improvement initiatives to reduce waste and enhance efficiency.
• Ensure compliance with quality standards and contribute to a culture of quality.

Requirements

• Nitec in Engineering
• No experience required; training provided.
• Comfortable working with microscopes.

Interview Process

• Face-to-face interview to understand the role.
• Theory test on Maths and English.
• Practical test using a microscope.

Interested candidate may submit full resume to (WhatsApp - Miya) and only shortlisted candidate will be notified.

By submitting your personal data and/or resume, you give consent to collection, use and disclosure of your personal data and/or resume by the company (or its agent) for the purpose of the processing and administration by the company relating to this job application.

Kuan Mei Yang

Registration Number: R

EA License No: 06C2859 (MCI Career Services Pte Ltd)

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Principal / Engineer, Innovation (Innovation Adoption), Medical Technology Office (Contract)
Job Category: Administration
Posting Date: 26 Jul 2025
As part of the innovation team, your role involves establishing processes and working to productise selected innovations including medical devices, software and AI medical devices for adoption within the SingHealth cluster. This includes collaborating with internal stakeholders and external manufacturing partners to implement these innovations in operational and clinical settings, while providing post-deployment technical support.
A key aspect of the role involves interfacing with end users and stakeholders to gather real-world implementation, clinical and cost-effectiveness data. This data supports impact assessment of adopted innovations and their eventual commercial potential. Additionally, the role encompasses defining, implementing and maintaining relevant processes and procedures under the office's ISO 13485-compliant quality management system.
Job Requirements
Bachelor’s Degree in Engineering or Science
2-4 years of relevant working experience in productisation, quality management systems, supply chain, enterprise IT and/or manufacturing
A Master’s Degree or PhD is advantageous
Experience in creating medical devices from project to marketed product
Experience in implementation/maintenance of a quality management system
Familiarity with ISO 13485, ISO 14971, IEC 62304, AI Medical Devices, Software-as-Medical-Device (SAMD), Medical Device Regulations, Medical Device Standards, Risk Management for Medical Devices
Knowledge of business or financing models for medical technology industries
Meticulous, responsible and self-motivated individual with excellent communication skills
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