15 Clinical Diagnostics jobs in Singapore

We are seeking a skilled professional to support and maintain Medical and Healthcare Software Application Systems.

This role involves performing user requirements analysis, application build and implementation, as well as conducting application system testing and support.

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Job Category: Administration

Posting Date: 2 Aug 2025

You will assist in the identification, validation and selection of unmet clinical needs, as well as participate in solution generation and prototyping. You will conduct testing, create supporting documentation required for patenting and regulatory approval and work with partners on commercialisation strategy.

You will coordinate and compile relevant information for grants and other funding applications, as well as manage and drive project tasks to ensure timely completion of project milestones. You will create relevant documentation, meeting records and support follow-up actions for clinical innovation projects.

You will support the device development team in brainstorming and prototype creation for projects. You will also be involved in general administrative and procurement assistance, and support the department in the program management of med-tech innovation grants including the grant application process, grant award and progress reporting.

You will provide administrative support for innovation training and education initiatives, including planning, implementation, publicity and events.

You will ensure compliance with quality, regulatory and organisation policies and systems, and support record-keeping and documentation needed for compliance.

Requirements

• Master’s / Bachelor’s Degree in Engineering, Biomedical Engineering or Science with preferably 2 years’ experience in medical technology innovation leading the development of concept ideas into products.
• Excellent team work and communication skills.
• Excellent problem solving skills with strong focus in technical writing.
• Strong knowledge in IT, CAD and/or Simulation Skills, e.g. LabView, MatLab, SolidWorks, AutoCad.
• Good knowledge in ISO 13485, ISO14155, Good Clinical Practice (GCP), Regulatory Affairs, Medical Device Standards, Intellectual Property Strategy will be an advantage.
• Knowledge of trial procedures, institutional, Centralised Institutional Review Board and regulatory authority (HSA) requirements will be an advantage.

• Participate in laboratory experiments involving PCR and serology tests
• Conduct routine workflows according to standard operating instructions
• Collaborate with team members to achieve project objectives
• Maintain accurate records and reports
• Ensure compliance with biosafety protocols

Requirements:

We are seeking candidates with the following qualifications:

• Diploma / Degree in Biomedical Sciences or related field
• Prior experience in a Life Sciences laboratory environment (an advantage)
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Good time management and organizational skills

Working Conditions:

The selected candidate will be required to work in a biosafety level 2 laboratory. Regular working hours will be 42 hours per week, and the contract duration is 6 months. We regret that only shortlisted candidates will be notified.

Senior Trade Compliance Analyst – Global Markets (Medical Technology Sector)

A global leader in the design, development, and manufacturing of advanced medical technologies that enhance patient care and improve lives is seeking a Senior Trade Compliance Analyst for the global markets.

As the committed Compliance professional dealing with quality, regulatory excellence, and responsible business practices, you must ensure that every product meets the highest standards of safety, compliance, and performance.

About the Role

We are looking for a highly motivated Senior Trade Compliance Analystto support and strengthen our clients international trade compliance program across key regions, particularly in JAPAC.

In this role, you will provide operational and strategic support in navigating complex global trade regulations — helping to ensure that life-changing medical technologies reach patients around the world efficiently and compliantly.

Reporting to the director, you will collaborate with global business units, supply chain teams, and regulatory stakeholders to uphold compliance with export control laws, customs regulations, and other trade-related requirements.

Key Responsibilities

• Provide day-to-day guidance and operational support on trade compliance issues, including export controls, sanctions, customs procedures, and product classification.

• Manage ECCN and HTS classifications, export licensing, and Country of Origin determinations.

• Assist in developing, updating, and enforcing global trade compliance policies and procedures.

• Monitor regulatory changes in the JAPAC region and assess business impact; recommend corrective or preventive actions as needed.

• Support internal audits, risk assessments, and continuous improvement of the trade compliance program.

• Work closely with Supply Chain, Regulatory, Legal, Logistics, and Quality teams to embed compliance into business processes and projects.

• Deliver tailored compliance training and awareness sessions to internal stakeholders across functions and geographies.

• Contribute to cross-border initiatives such as Free Trade Agreement (FTA) assessments and supply chain risk mapping, including forced labor prevention.

• Leverage SAP GTS and other Global Trade Management (GTM) tools to automate and monitor compliance workflows.

• Maintain accurate and auditable records in accordance with applicable trade regulations and internal policies.

• Serve as a liaison with government agencies and customs authorities across APAC, supporting inquiries, audits, and trade-related engagements.

Required/Preferred Qualifications

• Bachelor’s degree in International Trade, Business, Law, Logistics, or a related field.

• Minimum 5 years of experience in international trade compliance, ideally in the medical technology, pharmaceutical, or high-tech manufacturing sectors.

• Strong knowledge of Import/Export, HTS/ECCN classification, licensing, and APAC trade laws.

• Experience with SAP GTS or similar GTM platforms; familiarity with Oracle Cloud is a plus.

• Proficiency in Microsoft Office (Excel in particular).

• Excellent written and verbal communication skills.

• Highly detail-oriented, with strong problem-solving and prioritization abilities.

• Proven ability to work both independently and collaboratively in a fast-paced, global environment.

What’s On Offer

• A career within the Medical Technology sector delivering impactful technologies that improve lives.
  Newly created role and an opportunity to grow and lead compliance initiatives

• A collaborative, mission-driven culture that values expertise, ownership, and innovation

• Benefits, and professional growth opportunities.

• Global multinational organisation
  

What’s Next

If you’re looking to apply your expertise in trade compliance within a meaningful sector, we’d love to hear from you. Apply directly with your latest CV or send to us directly at

Note: Due to the high volume of applications, we may not be able to respond to everyone individually. If you do not hear from us, please assume your application was unsuccessful this time, but we encourage you to reapply in the future.

We look forward to considering your application!

Engage Group Life Science – Singapore & SEA


Engage Group Pte.Ltd is a licensed business under the Ministry of Manpower: (EA: 18C9316)

• Bachelor's Degree in Computer Engineering, Computer Science, Information Technology, Electrical Engineering or equivalent are preferred. Degree holders with a recognised Diploma in Cybersecurity/IT will also be considered
• At least 6 years of relevant working experience in the area of IT, Operations and Risk Management with medical devices/systems understanding
• Good understanding of both IT and BME processes/operations and the relationship between them is an advantage
• Good working knowledge of the best practices in mitigating security risks for IoMT medical devices/systems
• Experience in healthcare facilities projects and/or government projects will be an added advantage
• Possess strong communication, administrative, organisational and management skills
• Reliable team player, independent and committed

Reporting to the Assistant Director, you will execute administrative and operational activities that are critical to the operation of Internet of Medical Things (IoMT) activities for medical devices at one of SingHealth's institutions and coordinate and support cybersecurity strategies. You will collate and analyse information to facilitate management decisions and prepare reports for stakeholders. You will also work with the Biomedical Engineering (BME) shared services and IT security teams across SingHealth to ensure a robust risk management framework is in place for medical devices that are connected to the IT network. This includes updating the asset inventory, implementing the relevant standards and procedures for IoMT medical devices and evaluating and executing work instructions to minimise the risk for medical devices and systems. You will also provide secretariat support and participate in ad hoc projects.

Job Requirements

• Bachelor's Degree in Computer Engineering, Computer Science, Information Technology, Electrical Engineering or equivalent are preferred. Degree holders with a recognised Diploma in Cybersecurity/IT will also be considered
• At least 6 years of relevant working experience in the area of IT, Operations and Risk Management with medical devices/systems understanding
• Good understanding of both IT and BME processes/operations and the relationship between them is an advantage
• Good working knowledge of the best practices in mitigating security risks for IoMT medical devices/systems
• Experience in healthcare facilities projects and/or government projects will be an added advantage
• Possess strong communication, administrative, organisational and management skills
• Reliable team player, independent and committed

Reporting to the Assistant Director, you will provide administrative and operational support that are critical to the operation of Internet of Medical Things (IoMT) activities for medical devices at one of SingHealth's institutions to fulfil strategic priorities and initiatives across the cluster. You will collate and analyse information to facilitate management decisions and prepare reports for stakeholders. You will also work with the Biomedical Engineering (BME) shared services and IT security teams across SingHealth to ensure adequate risk oversight for medical devices and systems. This includes updating the asset inventory, support in implementation of relevant standards and good practices for IoMT medical devices, evaluating and executing work instructions and minimising risk for medical devices and systems. You will also provide secretariat support during meetings and participate in adhoc projects.

Requirements

• Bachelor's Degree in Computer Engineering, Computer Science, Information Technology, Electrical Engineering or equivalent are preferred. Degree holders with a recognised Diploma in Cybersecurity/IT will also be considered
• At least 2 years of relevant working experience in the area of IT, Operations and Risk Management with medical devices/systems understanding
• Good understanding of both IT and BME processes/operations and the relationship between them is an advantage
• Good working knowledge of the best practices in mitigating security risks for IoMT medical devices/systems
• Experience in healthcare facilities projects and/or government projects will be an added advantage
• Possess strong communication, administrative, organisational and management skills
• Reliable team player, independent and committed

Job ID: 4307

Job Function: Allied Health

Institution: National University Health System

Associate Medical Laboratory Technologists (AMLT) are responsible for the daily operations of the laboratory which include phlebotomy, electrocardiogram, spirometry and clinical laboratory work.

Responsibilities

1. Perform daily operations of the laboratory
2. Perform all procedures in accordance with laboratory standard operating procedures (SOPs)
3. Perform phlebotomy, Electrocardiogram (ECG) and spirometry in an accurate, efficient and professional way.
4. Perform Point of Care Testing (e.g. Prothrombin Time, glucose) and clinical laboratory tests such as urinalysis (e.g. Urine FEME, dipstick, pregnancy), haematology (e.g. full blood count, peripheral blood film, erythrocyte sedimentation rate, prothrombin time), biochemistry (e.g. HbA1c, neonate bilirubin), microscopy examination (e.g. fungal smear, high vaginal swab) independently.
5. Ensure specimen identification, processing and storage of test specimens are in consistent with good laboratory practices
6. Perform and verify quality control for all analysers prior to patients sampling
7. Use of Laboratory Information System (LIS) to perform functions such as result entry, result validation and tracking for outstanding tests
8. Ensure all test results provided for clinicians are accurate and reliable
9. Ensure analysers/equipment are functioning properly and are well maintained.
10. Notify medical technologist/lab in charge when instrument malfunction and make arrangements with BME or instrument vendor to service the instrument
11. Notify inventory person in charge when reagents and stocks supplies run low.
12. Perform and record internal and external quality controls and calibrations. Troubleshoot outliers in accordance to work instructions.
13. Ensure ‘critical value’ are reported to the relevant personnel within 30 minutes
14. Ensure daily maintenance and QC records are up to date.
15. Ensure compliance to hand hygiene, workplace safety, International Patient Safety Goals (IPSG) and International Standardization of Organizations (ISO) and other applicable regulatory and accreditation requirements of the laboratory.
16. Provide prompt and courteous service in person or over telecommunication to all external and internal customers (e.g patients, doctors, service providers, colleagues).
17. Report adverse incidents and all workflow anomaly to supervisor
18. Observe strict NUHS personal data protection act and observe internet/intranet cybersecurity guidelines.
19. Perform other functions as delegated by supervisor and/or lead laboratory

Requirements

Recognized Diploma in Biomedical Science, Clinical Laboratory Science or other relevant fields

At least 1-3 years of experience in laboratory environment and/or relevant experience in phlebotomy preferred

Good verbal and written communication skills

Ability to communicate in vernacular languages are an added advantage

Ability to multi-task and work in a fast-paced environment

Team player with good interpersonal skills

Associate Medical Laboratory Technologists (AMLT) are responsible for the daily operations of the laboratory which include phlebotomy, electrocardiogram, spirometry and clinical laboratory work.

Responsibilities

• Perform daily operations of the laboratory
• Perform all procedures in accordance with laboratory standard operating procedures (SOPs)
• Perform phlebotomy, Electrocardiogram (ECG) and spirometry in an accurate, efficient and professional way.
• Perform Point of Care Testing (e.g. Prothrombin Time, glucose) and clinical laboratory tests such as urinalysis (e.g. Urine FEME, dipstick, pregnancy), haematology (e.g. full blood count, peripheral blood film, erythrocyte sedimentation rate, prothrombin time), biochemistry (e.g. HbA1c, neonate bilirubin), microscopy examination (e.g. fungal smear, high vaginal swab) independently.
• Ensure specimen identification, processing and storage of test specimens are in consistent with good laboratory practices
• Perform and verify quality control for all analysers prior to patients sampling
• Use of Laboratory Information System (LIS) to perform functions such as result entry, result validation and tracking for outstanding tests
• Ensure all test results provided for clinicians are accurate and reliable
• Ensure analysers/equipment are functioning properly and are well maintained.
• Notify medical technologist/lab in charge when instrument malfunction and make arrangements with BME or instrument vendor to service the instrument
• Notify inventory person in charge when reagents and stocks supplies run low.
• Perform and record internal and external quality controls and calibrations. Troubleshoot outliers in accordance to work instructions.
• Ensure 'critical value' are reported to the relevant personnel within 30 minutes
• Ensure daily maintenance and QC records are up to date.
• Ensure compliance to hand hygiene, workplace safety, International Patient Safety Goals (IPSG) and International Standardization of Organizations (ISO) and other applicable regulatory and accreditation requirements of the laboratory.
• Provide prompt and courteous service in person or over telecommunication to all external and internal customers (e.g patients, doctors, service providers, colleagues).
• Report adverse incidents and all workflow anomaly to supervisor
• Observe strict NUHS personal data protection act and observe internet/intranet cybersecurity guidelines.
• Perform other functions as delegated by supervisor and/or lead laboratory

Requirements

• Recognized Diploma in Biomedical Science, Clinical Laboratory Science or other relevant fields
• At least 1-3 years of experience in laboratory environment and/or relevant experience in phlebotomy preferred
• Good verbal and written communication skills
• Ability to communicate in vernacular languages are an added advantage
• Ability to multi-task and work in a fast-paced environment
• Team player with good interpersonal skills