As our Clinical Laboratory Scientist, your role in setting up and being part of our laboratory operations would allow more people in the United States to access our advanced liquid biopsy technology.

With offices in Singapore, Hong Kong and Suzhou, joining Lucence means you will be part of an international and dynamic team striving towards our vision of a world without avoidable cancer deaths. It is important to us that every team member is aligned with the progress and goals of the company regardless of one’s physical location – this would require you to be comfortable accommodating international time zones for online company-wide events, cross-team discussions and remote training, when necessary.

Key responsibilities:

• Performing high complexity testing according to established SOPs for molecular diagnostic techniques, including nucleic acid extraction, PCR, genotyping, and next generation sequencing.
• Correctly receiving, requisitioning, processing, and ensuring proper identification of specimens and chain of custody.
• Evaluating sample integrity and adhering to relevant procedures in cases of unacceptable specimens.
• Setting up new laboratory equipment and performing equipment maintenance checks on a regular basis or as needed.
• Managing laboratory supplies and inventory.
• Participating in reagent and assay quality control and validations as needed.
• Participating in internal and external quality assurance programs.
• Troubleshooting assays and instruments as needed.
• Maintaining strict quality standards according to the laboratory’s accreditation standards, e.g. CAP, CLIA, ISO.
• Documenting all corrective actions taken should test systems deviate from the laboratory’s established performance specifications.
• Preparing for internal/external audits as needed.

To be a good fit for this role, you would have:

• At least a Bachelor’s degree in Biological Sciences, Life Sciences or a relevant field.
• An active California Clinical Laboratory Scientist license in good standing.
• At least 2 years of experience working in an accredited (e.g. CAP) clinical laboratory.
• Familiarity with molecular diagnostic techniques, especially next generation sequencing. Experience in liquid biopsy is advantageous.
• Familiarity with laboratory information management systems.
• Prior experience setting up a clinical molecular diagnostics laboratory would be highly advantageous.
• A high degree of attention to detail.
• Willingness to ‘roll your sleeves up’ and pave the way forward for constructive progress, even when the road ahead isn’t easy!

Specific title may be calibrated to match a given candidate’s experience.

Please send your CV to  [email protected] indicating the position you are applying for in the subject line. In addition, get creative and tell us in the email in less than 100 words (in any language you like) why you think you will be a right fit for Lucence. Don’t limit yourself to a job description or job title, the world needs every skill you have.

In this role, you will play an important part in the evaluation of genomic variants and ensuring that physicians and patients receive timely, accurate and comprehensive clinical reports based on our diagnostic tests.

Key responsibilities:

• Based on an in-depth understanding of Lucence’s Technology and Product portfolio and Medical Science, interpreting genomic alterations in appropriate clinical contexts and further developing rules for such interpretation.
• Database curation – evaluating scientific publications/clinical studies and integrating functional effects of genomic variants and their associated diseases using standard terminologies and established guidelines.
• Regularly updating the database with published clinical findings/publications.
• Writing, maintaining and updating workflows and protocols for clinical reporting pipeline.
• Working collaboratively with informatics and software team on creating and optimizing reporting workflows.
• Developing training programs for Medical Data Science at Lucence.
• Contributing scientific expertise to projects within the Research team.
• Participating in research-oriented projects for clinical validation of tests (in collaboration with external organizations).
• Participating in internal and external quality assurance programs.
• Performing other relevant duties as assigned.

To be a good fit for this role, you would have:

• PhD in Biomedical Science, Life Sciences, Cancer Biology, Genetics, Genomics or its equivalent.
• Working experience in research and development of molecular assays or cancer genomics and/or next-generation sequencing principles (we may also consider achievements and publications from your PhD course where relevant).
• Proficiency/strong understanding in molecular techniques, genetics and NGS applications.
• Excellent grasp of English with good communication and presentation skills and an ability to write short summary reports.
• Exceptional attention to detail.

The following will be a plus:

• Knowledge in genomic medicine and liquid biopsy.
• Fluency in variant annotation and interpretation and use of genome databases such as COSMIC, ClinVar, Varsome, Ensembl and OncoKB.
• Ability to interpret genomic data in patient- and treatment-specific contexts following established procedures.
• Track record of publishing.

Specific title and responsibilities may be calibrated to match a given candidate’s experience.

Please send your CV to [email protected] indicating the position you are applying for in the subject line. In addition, get creative and tell us in the email in less than 100 words (in any language you like) why you think you will be a right fit for Lucence. Don’t limit yourself to a job description or job title, the world needs every skill you have.

Key responsibilities:

• Processing specimens, analyzing data and reporting results accurately following established procedures and with the strictest adherence to safety procedures.
• Troubleshooting and resolving technical problems.
• Conducting technical and clinical verification and validation studies.
• Participating in internal and external quality assurance programs.
• Monitoring inventory and lab supplies in assigned areas.
• Performing other duties as assigned to ensure smooth laboratory operations.

To be a good fit for this role, you would have:

• At least a degree in Biomedical Science, Life Sciences or its equivalent.
• Familiarity with molecular diagnostics techniques, including handling of patient samples, nucleic acid extraction, real-time PCR, genotyping and sequencing etc.
• Flexibility in working on weekends, public holidays, morning shifts (e.g. 7am-4pm) and afternoon shifts (e.g. 12pm-9pm) as needed, based on staff rosters.
• The ability to work independently as well as in a team.
• Exceptional attention to detail as meticulousness is key when dealing with patient samples.
• Strong self-motivation, resilience, keen interest in learning and the ability to work well under pressure.

Specific title and responsibilities may be calibrated to match a given candidate’s experience.

Please send your CV to [email protected] indicating the position you are applying for in the subject line. In addition, get creative and tell us in the email in less than 100 words (in any language you like) why you think you will be a right fit for Lucence. Don’t limit yourself to a job description or job title, the world needs every skill you have.

Key responsibilities:

• Processing specimens, analyzing data and reporting results accurately following established procedures.
• Designing, planning and performing laboratory molecular tests, in particular, next generation sequencing (NGS).
• Troubleshooting and resolving technical problems.
• Optimizing new genomic medicine technologies.
• Conducting technical and clinical verification and validation studies.
• Participating in internal and external quality assurance programs.
• Monitoring inventory and lab supplies in assigned areas.
• Performing other duties as assigned to ensure smooth laboratory operations.

To be a good fit for this role, you would have:

• At least a degree in Biomedical Science, Life Sciences or its equivalent. (PhD holders may be considered for senior roles.)
• Familiarity with molecular diagnostics techniques, including handling of patient samples, nucleic acid extraction, real-time PCR, genotyping and sequencing etc. (Experience in NGS is a plus.)
• Flexibility in working on weekends, public holidays, morning shifts (e.g. 7am-4pm) and afternoon shifts (e.g. 12pm-9pm) as needed, based on staff rosters..
• The ability to work independently as well as in a team.
• Exceptional attention to detail as meticulousness is key when dealing with patient samples.
• Strong self-motivation, resilience, keen interest in learning and the ability to work well under pressure.

Specific title and responsibilities may be calibrated to match a given candidate’s experience.

Please send your CV to [email protected] indicating the position you are applying for in the subject line. In addition, get creative and tell us in the email in less than 100 words (in any language you like) why you think you will be a right fit for Lucence. Don’t limit yourself to a job description or job title, the world needs every skill you have.

Key responsibilities:

• Being the key personnel managing specimen receipt in our clinical laboratory. Day-to-day duties include data entry of specimen details when specimens are delivered to us, scanning and filing of specimen order forms, communicating with the Sales team when clarifications are needed and keeping track of follow-ups.
• Assisting in specimen processing steps.
• Assisting in ensuring smooth logistics and workflow of international deliveries of specimens to our laboratory. This would involve identifying packaging and delivery requirements for specimens from overseas markets (e.g. the US) and tracking of delivery status.

Specimens are received at our laboratory for cancer diagnostics and COVID-19 testing. Please note that you will not be coming into direct contact with any of the specimens, but you should be comfortable handling the kits, blood tubes etc. that contain such specimens. These would include blood/tissue samples for cancer-related tests and swab/saliva samples for Covid-19 tests.

To be a good fit for this role, you would have:

• At least a diploma. Experience managing operational matters in a related field (e.g. biological sciences, molecular biology, genetics) is a plus.
• Flexibility in working on weekends, public holidays, morning shifts (e.g. 7am-4pm) and afternoon shifts (e.g. 12pm-9pm) as needed, based on staff rosters.
• Exceptional attention to detail, being highly meticulous and organized. This is an administrative role that is a crucial part of our workflow.
• The ability to think creatively for novel solutions to day-to-day challenges.
• Strong interpersonal and communication skills
• The ability to work with others in a positive and collaborative manner to meet organizational goals.
• The ability to work well and accurately in a fast-paced environment.

Specific title and responsibilities may be calibrated to match a given candidate’s experience.

Please send your CV to [email protected] indicating the position you are applying for in the subject line. In addition, get creative and tell us in the email in less than 100 words (in any language you like) why you think you will be a right fit for Lucence. Don’t limit yourself to a job description or job title, the world needs every skill you have.

Key responsibilities:

Laboratory

• Conducting experiments based on established standard operating procedures while maintaining stringent safety and quality standards.
• Troubleshooting and improving test assays involved with QC requirements.
• Laboratory equipment maintenance and inventory management, as necessary.
• Quality controls for our molecular assays and/or our reagents, to ensure the efficacy of Covid-19 sample collection kits.

Quality Management

• Ensuring a robust and effective QMS (quality management system) through monitoring and reviewing quality metrics and compliance.
• Identifying, implementing, and managing quality metrics in a process of continual improvement.
• Logistical management to ensure a sufficient supply of abovementioned collection kits (quality assured) based on orders.
• Maintaining all necessary quality documentation (e.g. product specifications, standard operating procedures) in adherence with clinical and accreditation standards.

To be a good fit for this role, you would have:

• At least a bachelor’s degree in Biomedical Science, Life Sciences, or a relevant field.
• Experience working in a regulated laboratory environment (ISO/CAP) or a clinical/molecular laboratory setting in a quality role would be advantageous.
• Familiarity with molecular diagnostic techniques, including nucleic acid extraction, PCR, genotyping, and sequencing.
• Exceptional attention to detail.
• Proactiveness in evaluating improvements in processes and implementing them.

Specific title and responsibilities may be calibrated to match a given candidate’s experience.

Please send your CV to [email protected] indicating the position you are applying for in the subject line. In addition, get creative and tell us in the email in less than 100 words (in any language you like) why you think you will be a right fit for Lucence. Don’t limit yourself to a job description or job title, the world needs every skill you have.

Key responsibilities:

• Collaborating with cross-functional teams to define, design and build high-quality web applications/services.
• Enhancing existing data operation systems by analyzing business objectives, architecting and developing applications across platforms.
• Maintaining existing software systems by identifying and correcting software defects.
• Continuously discovering, evaluating and implementing new web technologies to improve development efficiency.
• (For front-end developer especially) Leading front-end testing of our web applications/services and applying UX/UI insights for better user experience.

To be a good fit for this role, you would have:

• A Bachelor’s degree or above in Computer Science, Mathematics, Engineering, or related disciplines.
• A strong passion for building software and a keen interest in creating solutions for real-time healthcare problems.
• Fluency in server-side programming languages, such as Java, python, golang.
• Familiarity with HTML, CSS, JavaScript; experience in Angular/React/Vue will be advantageous.
• Familiarity with relational databases, such as MySQL, PostgreSQL.
• Prior relevant working experience would be an advantage.

Please send your CV to [email protected] indicating the position you are applying for in the subject line. In addition, get creative and tell us in the email in less than 100 words (in any language you like) why you think you will be a right fit for Lucence. Don’t limit yourself to a job description or job title, the world needs every skill you have.

Shortlisted candidates for this role will be invited to try out our coding tasks for further shortlisting.

Key responsibilities:

• Developing novel algorithms and statistical models as required by the company.
• Building production-level bioinformatics pipelines using docker and AWS step functions.
• Developing databases to compile vast amounts of genomic and diagnostics information.

To be a good fit for this role, you would have:

• A Bachelor’s degree, Master’s degree or PhD in Bioinformatics/ Computational Biology/ Computer Science or the equivalent.
• Experience developing bioinformatics algorithms or software independently.
• Strong proficiency in programming (Python, R, Unix shell scripts).
• A good understanding of biology, algorithms and statistics.
• Strong self-motivation with an inquisitive mind and a keen interest in creating solutions for real-time healthcare problems.

Please send your CV to [email protected] indicating the position you are applying for in the subject line. In addition, get creative and tell us in the email in less than 100 words (in any language you like) why you think you will be a right fit for Lucence. Don’t limit yourself to a job description or job title, the world needs every skill you have.

Shortlisted candidates for this role will be invited to try out our coding tasks for further shortlisting.