380 Laboratory Scientist jobs in Singapore

• 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.

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 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 Description:

- Manages daily team activities, prioritising specimens and overseeing testing and reporting

- Supervises staff, providing training, competency assessments, and addressing disciplinary matters

- Maintains and troubleshoots laboratory equipment, including calibration and quality control.

- Manages incidents, assists investigations, and implements corrective actions.

- Develops and reviews laboratory documentation, including policies and work instructions.

- Utilises laboratory information systems and relevant software

- Oversees personnel performing tests and reporting results, ensuring adherence to guidelines

- Perform specimen reception, order entry and other duties in the laboratory as assigned

Job Requirements:

- Minimum Degree in Biomedical Science

- ASCPi certified preferred

- Minimum 4 years of experience in working in a clinical laboratory

- Experience in biochemistry preferred

- Experience in a healthcare setting preferred

- Experience in training and assessment of staff, writing and implementing policies and instructions preferred

All qualified applicants, please send in your resume to:

Tricia Celestine Goh (R )

Recruit Express Pte Ltd | Company Reg. No. W | EA License Number: 99C4599

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.

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.