422 Laboratory Scientist jobs in Singapore

• 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

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.

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.

KK Women’s and Children’s Hospital (KKH) is an 830-bed tertiary-level care hospital that provides obstetrics, gynaecology, neonatology and paediatric healthcare services. It is part of the SingHealth public healthcare cluster and is an academic medical centre. KKH is a major teaching hospital for Duke-NUS Medical School, Yong Loo Lin School of Medicine and Lee Kong Chian School of Medicine.

The Department of Pathology and Laboratory Medical at KKH strives to achieve the highest standards in providing clinical services to a wide range of patients.

You will be part of the Clinical Chemistry team, providing scientific and technical input to the operation, management and development of the Clinical Chemistry laboratory in the department.

Job Requirements:

• Bachelor of Science in Biomedical Science, Biological Science, Medical Technology or equivalent.
• Minimum 3 years of work experience in a clinical biochemistry laboratory.
• Experience with laboratory accreditation requirement & handling of quality assurance programmes.
• Ability to work shifts, including nights, weekends, public holidays and for on-call standbys.
• You must be scientifically vigorous, eager to learn and willing to work in a fast-paced, clinical environment.

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.
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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.

Job Title: Laboratory Scientist

• The laboratory scientist will collect and analyze laboratory experimental data in a safe and timely manner.
• The ideal candidate must be proficient in operating construction lab equipment such as Instron, Sealant mixing pump, aging chambers, dispensing guns.
• The successful applicant should be able to perform application testing independently for silicone sealants.
• S/he will support project management system related lab work to ensure timely technical service.

• Candidates must possess at least a Diploma / Degree in Science / Chemistry / Engineering or any other related discipline.
• A minimum of 2 years of working experience in chemical Lab is highly desirable.
• Experience of working on analytical equipment will be advantageous.

Skills Required:

• Excellent communication and teamwork skills.
• Ability to maintain accurate records and report results.
• Problem-solving skills and attention to detail.

Benefits:

• Ongoing training and development opportunities.
• Competitive salary and benefits package.