126 Medical Laboratory jobs in Singapore

Job ID: 8282

Job Function: Allied Health

Institution: National University Hospital

NCIS is establishing a new Stem Cell Therapy Hub (SCTH) as part of its expansion of specialised programmes, aiming to become a Reference Centre of Excellence. We are seeking a Quality Control (QC) Specialist for the QC department.

The candidate will perform assigned Quality Control Testing, including Raw Material Testing, In-process testing, Final Product Testing, and other analytical activities related to Cellular Therapy and Haematopoietic Stem Cell Transplant services.

• Perform routine analytical, microbiological, and environmental testing based on assigned technical roles.
• Coordinate and schedule testing activities.
• Ensure availability of critical materials, reagents, and consumables.
• Coordinate procurement and provide User Requirements Specifications (URS) for QC materials.
• Manage sample and QC material shipments.
• Ensure laboratory operations comply with cGMP procedures, including test execution, review, and data documentation.
• Participate in SOP creation, review, equipment qualification, and method validation activities.
• Coordinate and perform calibration and preventive maintenance of laboratory equipment.
• Initiate quality documents such as investigations, deviations, and change controls when necessary.
• Support issue resolution, discrepancy investigations, and CAPA implementation.
• Assist in reviewing protocols, reports, SOPs, and other documents.
• Participate in method validation and verification activities, including protocol preparation and review.
• Perform trend analysis of test data for monitoring purposes.
• Conduct training as a subject matter expert on test methods, systems, and equipment.
• Support improvement initiatives within the Quality Management System.
• Assist during internal and external audits/inspections as a subject matter expert.
• Escalate quality and compliance risks to QC Management and QA.
• Perform other responsibilities as assigned by QC Management.

• Bachelor's degree or higher in Science, Pharmacy, Pharmaceutical Science, or related fields; 2-4+ years of relevant QC experience in the pharmaceutical, biotech, medical device, or healthcare industry preferred.
• Strong knowledge of quality control, quality management systems, and validation requirements, with experience in vendor management advantageous.
• Understanding of regulations and industry guidance, especially for stem cell, gene, and cell therapies.
• Effective communication skills and stakeholder engagement across functions.
• Critical thinking and problem-solving skills are advantageous.

• Perform and supervise medical laboratory tests across various disciplines in laboratory medicine.

• Ensure accuracy, reliability, and timely reporting of test results.

• Oversee daily laboratory operations, including workflow management, troubleshooting, and staff guidance.

• Maintain and enforce compliance with quality control, safety, and regulatory standards.

• Ensure optimal functioning, calibration, and maintenance of laboratory equipment.

• Collaborate closely with physicians, nurses, and other healthcare professionals to support clinical decision-making.

• Contribute to the training and development of junior laboratory staff.

Requirements:

• Bachelor’s degree in Medical Laboratory Science or a related field; advanced degree is an advantage.

• Relevant professional certifications and licenses required for medical laboratory practice in Singapore.

• Proven experience in Laboratory Medicine and Pathology.

• Proficient in Medical Technology, laboratory skills, and Quality Control practices.

To submit your application, please apply online to

Your interest will be treated with the strictest of confidence. We regret that only shortlisted candidates will be notified or contacted.

RN Care Pte. Ltd
EA License No: 17C8900

You will perform laboratory tests, assist in preparing various types of media as well as receive and process specimens, including carrying out specialised investigations of patient samples. In addition, you will perform on-going quality control checks to ensure test results are precise and accurate.

Job Requirements

• Degree in Biomedical Science, Life Sciences or its equivalent
• Able to work independently as well as a team

Reporting to Centre-IC, the Medical Laboratory Technologist (MLT) is responsible for the daily operations and administration of laboratory to ensure compliance to regulations and accreditation standards. This includes daily routine laboratory work, performing phlebotomy, electrocardiogram and spirometry. The MLT is responsible to maintain professional care to patients and works closely with NUP and other stakeholders.

Job scope

• Perform patient registration, specimen reception, preparation and packing of specimens
• Perform laboratory analysis (e.g. Urine microscopy, full blood count, HbA1c), operate and maintain instruments according to work instruction.
• Perform point-of-care testing, phlebotomy, ECG and spirometry procedures.
• Responsible to verify and report accurate results in timely fashion; investigates and reports any anomalies.
• Responsible to perform daily quality control check and troubleshoot as required.
• Ensure proper documentations and records for traceability (e.g. acknowledgement on QC and maintenance checklist after completion).
• Assist to resolve patient’s queries and escalate to centre-IC when necessary.
• Adhere to work safety guidelines and infection control protocols to ensure staff and patient safety.
• Assist centre-IC in tasks as assigned.

Qualification

• Degree in Medical Laboratory/Biomedical Science or related fields.
• Prior experience working at clinical laboratory at public or private healthcare establishment is advantageous but training will be provided
• Experience in phlebotomy and heel prick sample collection will be advantageous but training will be provided
• Effective communications and ability to converse in vernacular languages is an asset
• Able to work in a fast-paced environment and with good problem solving skills
• Possess positive attitude in resolving hostile and disgruntled patients professionally
• Ability to multi-task and work under tight timelines
• Good interpersonal relationship skills and enjoy working as a team
• Computer literate – knowledge of MS Word, Excel and PowerPoint will be advantageous
• 5.5 Days work week (830-430pm) / (830-1230pm)

Only shortlisted candidates will be notified

EnviroDynamics Solutions Pte Ltd I EA License No.: 12C6285

Karen Koh I Reg. No: R1108844

Email CV to : karenkoh @envirodynamics.com.sg

Responsiblities:

• Perform phlebotomy procedures using proper, sterile, and safe techniques.:
• Perform venepuncture only (no arterial), up to a maximum of two attempts. Refer difficult cases to clinician.
• Project friendly, approachable and caring personality towards patients.
• Prepare specimens and test requests for despatch to referral laboratories.
• Prepare completed laboratory reports for despatch to external clients.
• Receive laboratory consumables and other items, and store them appropriately.

Other

• Assist Laboratory Manager in promoting safety in the laboratory.
• Involved in hospital activities including participation in Continuous Improvement Programme.
• Participate in community outreach programmes.

Job Requirements:

• Minimum 5 GCE “O” levels or equivalent
• Diploma in Biotechnology or Biomedical related will also be considered

Overview*

NCIS is establishing a new Stem Cell Therapy Hub (SCTH) as part of expansion of its Specialized Programmes and to become a Reference Centre of Excellence. We are looking for a Quality Control (QC) Specialist for the QC department in the organization.

The candidate will execute the assigned Quality Control Testing (e.g. Raw Material Testing, In-process testing, Final Product Testing, Analytical Science and Technology, Environmental and QC Systems, for NCIS Specialized Programmes (specifically Cellular Therapy and Haematopoietic Stem Cell Transplant) and other provided services.

Job Responsibilities*

• Responsible for routine testing which includes analytical, bioanalytical, microbiological and/or environmental samples testing, depending on the technical role assigned.

• Coordinating and scheduling of testing activities.

• Ensure all critical materials, reagents and consumables required for testing are available.

• Coordinate procurement and provide URS of materials for QC usage which includes consumables, reagents, test media, test cultures, small equipment, glassware, plasticware etc.

• Coordinate shipment of samples and QC materials.

• Ensure all laboratory operations including test execution, review and data documentation are performed according to cGMP procedures.

• Participate in creating SOP, reviewing SOP, equipment qualification and method verification/validation activities.

• Coordinate/Perform calibration and preventive maintenance of laboratory equipment

• Initiate quality document such as out of specification investigation, deviation record, change control etc if necessary.

• Support in the timely resolution of issues, including discrepancies, investigations and implementation of CAPAs.

• To support supervisor/manager in reviewing protocols/reports/SOPs and other documents assigned by the supervisor/manager.

• Participate in method validation/method verification activities which include protocols preparation and review.

• Perform trend analysis of test data that are essential for monitoring purpose.

• To conduct training as subject matter expert in the test methods, systems and equipment assigned.

• Supports improvement initiatives, programs and projects driven from the Quality Management System

• Support as subject matter expert during internal and external audits/inspections.

• Escalates quality and compliance risks to QC Management and QA.

• Any other responsibilities assigned by the QC Management

• Note: Other responsibilities may be assigned.

Requirements*

• Bachelor or higher, in Science, Pharmacy, Pharmaceutical Science, or equivalent, with preference of more than 2-4 years of relevant work experience in Quality Control role in the pharmaceutical/biotechnology/medical device/healthcare industry.

• Good knowledge of quality control, quality management system and validations requirement, preferably with third party customer/supplier or vendor management experience.

• Good knowledge in regulations and industrial guidance especially for stem cell / cell and gene therapy

• Good communication and able to engage stakeholders effectively from different functional units

• Critical thinking and problem-solving skill are of advantage.

Reporting to Centre-IC, Medical Technologist (MT) is responsible for the daily operations and administration of laboratory to ensure compliance to regulations and accreditation standards. This includes daily routine laboratory work, performing phlebotomy, electrocardiogram and spirometry. MT is responsible to maintain professional care to patients and works closely with NUP and other stakeholders.

Job scope

• Perform patient registration, specimen reception, preparation and packing of specimens
• Perform laboratory analysis (e.g. Urine microscopy, full blood count, HbA1c), operate and maintain instruments according to work instruction.
• Perform point-of-care testing, phlebotomy, ECG and spirometry procedures.
• Responsible to verify and report accurate results in timely fashion; investigates and reports any anomalies.
• Responsible to perform daily quality control check and troubleshoot as required.
• Ensure proper documentations and records for traceability (e.g. acknowledgement on QC and maintenance checklist after completion).
• Assist to resolve patient’s queries and escalate to centre-IC when necessary.
• Adhere to work safety guidelines and infection control protocols to ensure staff and patient safety.
• Assist centre-IC in tasks as assigned.

Qualification

Degree in Medical Laboratory/Biomedical Science or related fields.

Prior experience working at clinical laboratory at public or private healthcare establishment is advantageous but training will be provided

Experience in phlebotomy and heel prick sample collection will be advantageous but training will be provided

Effective communications and ability to converse in vernacular languages is an asset

Able to work in a fast-paced environment and with good problem solving skills

Possess positive attitude in resolving hostile and disgruntled patients professionally

Ability to multi-task and work under tight timelines

Good interpersonal relationship skills and enjoy working as a team

Computer literate – knowledge of MS Word, Excel and PowerPoint will be advantageous

Note : Candidates who are looking for Full Time/Part Time employment are welcome to submit the job application to us

Job ID: 7774

Job Function: Allied Health

Institution: National University Hospital

Overview

NCIS is establishing a new Stem Cell Therapy Hub (SCTH) as part of the expansion of its Specialized Programmes (specifically Cellular Therapy and Haematopoietic Stem Cell Transplant) and to become a Reference Centre of Excellence. We are looking for a Sr Medical Laboratory Scientist, who will be responsible for performing Cell, Tissue, and Gene Therapy (CTGT) Product manufacturing and interpreting product quality assurance testing results in the department. He/She is also responsible for undertaking related laboratory and manufacturing activities to ensure smooth lab and manufacturing services.

Job Responsibilities

1. Perform manufacturing procedures in accordance with cGMP, environmental health and safety guidelines and any other related regulations which could apply.
2. Perform routine QC and in-process testing sampling of the CTGT products at various stages throughout manufacturing (e.g., bioburden sampling, water sampling).
3. Timely completion of relevant manufacturing batch records and logbooks for the tasks performed with adherence to Good Documentation Practice (GDP).
4. Perform cleaning and upkeep of the equipment and classified area in manufacturing areas as per SOPs.
5. Report procedure deviations, adverse and out-of-specification incidents to the supervisor.
6. Undertake simple preventative maintenance and calibration of equipment in the facilities to ensure proper working conditions.
7. Participate in laboratory administrative work such as filing, processing of delivery orders, and invoices.
8. Support new manufacturing and quality control processes under the supervision of Manufacturing Lead (IQ, OQ, PQ, and PV).
9. Support the investigation, change control, and root cause investigations.
10. Any other duties as assigned by the supervisor.

Requirements

1. Bachelor’s Degree in Engineering (Chemical/Biomedical), Biotechnology, Life Science, or equivalent. Post Graduate Diploma or Professional Degree will be considered an advantage.
2. 3 to 5 years of relevant experience in the biopharmaceutical and/or medical device manufacturing industry and prior technical knowledge in batch biopharmaceutical processing will be an advantage.
3. Cleanroom with sterile and aseptic processing knowledge and experience.
4. Good understanding of safe working practices and cGMP.
5. Highly motivated to work in the pharmaceutical industry.
6. Demonstrated ability to elevate issues effectively and apply appropriate corrections.
7. Highly motivated, proactive, and enthusiastic team player with a demonstrated history of flexibility.
8. Ability to work independently, collaborate cross-functionally, and utilize resources efficiently.
9. Able to provide feedback for operations and elevate concerns as needed.
10. Excellent organizational, interpersonal, verbal, and written communication skills.
11. Able to work rotating shifts.
12. Good laboratory skills.
13. Above average dexterity with good general health and must be able to differentiate colors for work purposes.
14. Basic computer literacy.
15. Service-oriented and customer-focused.

Job ID: 7794

Job Function: Allied Health

Institution: National University Hospital

Overview*

To perform laboratory diagnostic procedures and related activities so as to provide a quality laboratory service to our customers, both internal and external.

Job Responsibilities*

Primary Responsibilities and Duties (80%)

1. Receive laboratory specimens and reject those that are unsuitable for analysis.
2. Operate the Laboratory Information System to perform functions such as result query, order entry and result entry.
3. Perform waived tests and moderate complexity tests. Perform all procedures in accordance with laboratory protocols.
4. Alert appropriate laboratory personnel of critical values.
5. Report any adverse incidents to senior member of staff.
6. Prepare reagents and materials that require special handling to ensure reliability.
7. Receive and resolve queries from customers.
8. Undertake preventive maintenance on laboratory instrumentation. Notify appropriate laboratory personnel when laboratory instruments malfunction.
9. Notify appropriate laboratory personnel when test kits, reagents or other supplies should be re-ordered.
10. Perform shift duties as required.
11. Keep current with new instrumentation, techniques and procedures by attending/participating in appropriate workshops, seminars and in-service education classes.
12. Promptly carry out the instruction(s) of senior staff with regard to work procedures and duties.
13. Comply with good laboratory practice as set out by the Laboratory Accreditation Programme of the College of American Pathologists and Singapore regulatory agencies such as the Medical Audit & Accreditation Unit.
14. Comply with all requirements of the Laboratory Safety Manual.
15. Comply with DLM Workplace Etiquette in line with NUHS Core Values.

Secondary Duties and Responsibilities (20%)

1. Demonstrate laboratory procedures to trainees and new staff.
2. Guide Laboratory Technicians, Clerical Staff and Health Attendants in their work when required.
3. Participate in routine laboratory administrative work such as filling, processing of deliveries orders and invoices.
4. Any other duties as assigned by supervisor.

Requirements*

Qualification Required and Area of Discipline

1. Diploma in Medical Laboratory Science.

Required Competencies and Capabilities (Skills, Experiences and Professional Licences)

1. Preferably with 1-2 years Clinical Laboratory experience.
2. Good laboratory skills.
3. Good general health and no colour blindness.
4. Basic computer skills.
5. Good initiative and attitude.
6. Good communication and interpersonal skills.