198 Medical Laboratory Scientist jobs in Singapore

A Variant Scientist position is available at KK Women's and Children's Hospital (KKH) for experienced candidates with experience in clinical genetics and clinical variant interpretation. The successful candidate will be part of the team responsible for analysis and interpretation of genetic variation identified by internal and external laboratories, with the aim of delivering accurate and comprehensive clinical genetic testing reports to patients and their care providers.

Other responsibilities include:

• Prepare relevant information for multidisciplinary team (MDT) meetings to enable proper classification of variants.
• Ensure the in-house database of genetic variants is kept up to date, and that periodic variant re-analysis is performed.
• Work closely with the bioinformatics team to develop and improve bioinformatics workflows.
• Provide domain knowledge expertise and training on variant curation best practices to colleagues of all levels.
• Participate in the writing of scientific publications to ensure that novel findings are disseminated.

Requirements

• Master of Science in a life sciences-related field or relevant qualification.
• Minimum of 3 years' experience (either in a research or clinical laboratory) with relevant work experience, including molecular genetics.
• Previous experience and proficiency in the application of variant classification guidelines (e.g., ACMG) would be advantageous.
• Proficiency in molecular biology, clinical genetics is relevant.

We regret to inform that only shortlisted candidate will be notified via email.

Job Description & Requirements

• Receive, examine and perform laboratory testing on clinical specimens and report the results within TAT in accordance with laboratory policies and standard operating procedures.
• Perform PCR, hybridisation, library preparation, next generation sequencing, as well as a variety of advanced genetic laboratory applications.
• Review results to determine interference, inhibition, or other problems that arise during extraction, amplification or sequencing of nucleic acids.
• Perform quality control, validation, and other activities to verify the performance of clinical assays.
• Perform routine maintenance and calibration of laboratory equipment, and notify Laboratory Manager when instruments malfunction.
• Work closely with Laboratory Manager/Director to ensure compliance with accreditation standards and regulatory requirements.
• Participate in quality assurance according to established policies and procedures.
• Manage inventory of supplies and reagents and communicate order needs.
• Operate computer programs related to equipment and LIS systems.
• Maintain records of test results and archives of data.
• Keep Good Clinical Practice and safe working environment complying with the requirements of laboratory safety, staff safety, and patient safety.
• Perform laboratory procedures, examinations, and other tests according to established laboratory policies and procedures.
• Maintain and demonstrate technical competence.

Preferred Skills/Qualifications

Education: Diploma in Medical Laboratory Technology or an equivalent qualification; or a basic degree in a relevant science subject

Experience: Preferably 2-3 years of clinical laboratory experience in molecular genetics, biochemical genetics, or cytogenetics. Keen interest to learn with positive work attitude, analytical thinking, good communication and interpersonal skills.

This list of duties and responsibilities is not all-inclusive and may be expanded to include other duties and responsibilities, as deemed relevant to the role. Salary will be commensurate with relevant experiences.

Job ID: 3763

Job Function: Allied Health

Institution: National University Health System

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

Job Scope

1. Perform patient registration, specimen reception, preparation, and packing of specimens.
2. Perform laboratory analysis (e.g. Urine microscopy, full blood count, HbA1c), operate and maintain instruments according to work instructions.
3. Perform point-of-care testing, phlebotomy, ECG, and spirometry procedures.
4. Verify and report accurate results in a timely fashion; investigate and report any anomalies.
5. Perform daily quality control checks and troubleshoot as required.
6. Ensure proper documentation and records for traceability (e.g. acknowledgment on QC and maintenance checklist after completion).
7. Assist in resolving patient queries and escalate to centre-IC when necessary.
8. Adhere to work safety guidelines and infection control protocols to ensure staff and patient safety.
9. Assist centre-IC in tasks as assigned.

Qualifications

1. Degree in Medical Laboratory/Biomedical Science or related fields.
2. Prior experience working in a clinical laboratory at a public or private healthcare establishment is advantageous but training will be provided.
3. Experience in phlebotomy and heel prick sample collection will be advantageous but training will be provided.
4. Effective communication skills and ability to converse in vernacular languages is an asset.
5. Able to work in a fast-paced environment with good problem-solving skills.
6. Possess a positive attitude in resolving issues with hostile and disgruntled patients professionally.
7. Ability to multi-task and work under tight timelines.
8. Good interpersonal relationship skills and enjoy working as a team.
9. 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 their job application to us.

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: 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.

Medical Laboratory Technologist / Sr Medical Laboratory Scientist (QC), NCIS
Job ID: 8282
Job Function: Allied Health
Institution: National University Hospital
Overview
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.
Job Responsibilities
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.
Requirements
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.
#J-18808-Ljbffr

Overview

NCIS is establishing a new Stem Cell Therapy Hub (SCTH) as part of 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 of Cell, Tissue, and Gene Therapy (CTGT) Product manufacturing and interpreting product quality assurance testing results in the department. He/She is also responsible to undertake related laboratory and manufacturing activities to always ensure smooth lab and manufacturing services.

Job Responsibilities

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

Requirements

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

Overview

NCIS is establishing a new Stem Cell Therapy Hub (SCTH) as part of 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 of Cell, Tissue, and Gene Therapy (CTGT) Product manufacturing and interpreting product quality assurance testing results in the department. He/She is also responsible to undertake related laboratory and manufacturing activities to always ensure smooth lab and manufacturing services.

Job Responsibilities

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

Requirements

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

Overview

NCIS is establishing a new Stem Cell Therapy Hub (SCTH) as part of 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 of Cell, Tissue, and Gene Therapy (CTGT) Product manufacturing and interpreting product quality assurance testing results in the department. He/She is also responsible to undertake related laboratory and manufacturing activities to always ensure smooth lab and manufacturing services.

Job Responsibilities

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

Requirements

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