743 Research jobs in Singapore

The Opportunity

Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.

Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.

Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.

Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which often we use cells as the factory to derive our target product.

Our first commercial breakthrough success is Esco Aster is commercially first in class being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.

We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.

The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.

Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.

Esco Aster.

One World Biosolutions for One Health.

Who we’re looking for

Physical/Mental Requirements/Work Environment

· Ability to read, analyze and interpret scientific data and publications.

· Ability to author or review protocols, technical reports and technology transfer documents.

· Ability to author and review standard operating procedures, batch records, protocols, data, reports and other related documents.

· Ability to define problems, collect data, establish facts, and draw conclusions.

· Repetitive motions due to certain laboratory techniques.

· Ability to adapt and keep up with rapid changes in a fluid and dynamic environment as this is a rapidly evolving space.

The Scope

You will be part of Esco Aster’s scientific division and contribute to the company’s CDMO mission and objectives. You will perform research and process development activities, in various projects and in collaboration with internal and external stakeholders, clients and partners.

Primary Work Location: Ayer Rajah Crescent, Singapore

Job Responsibilities

Design and Independently Execute Experiments:

· Design and laboratory-scale experiments to support client upstream processes and requests.

· Perform assay development and data analysis.

Upstream Process Evaluation and Optimization:

· Evaluate and optimize existing client processes in preparation for scale-up.

· Propose improvements and modifications to enhance process efficiency.

Scale-Up and Technology Transfer:

· Conduct scale-up experiments in larger bioreactors.

· Adapt processes to align with available on-site equipment.

· Facilitate technology transfer from clients, aiming at scaling up processes or implementing new technologies (e.g., perfusion, serum replacements).

Continuous Process Improvement:

· Proactively identify opportunities for process improvements.

· Initiate and drive enhancements to streamline processes.

Project Management and Documentation:

· Write client proposals, outlining milestones, timelines, and budgets for scale-up projects.

· Take ownership and accountability for all deliverables and milestones in assigned projects.

· Summarize project work in a formal report and communicate effectively to stakeholders.

Cross-Functional Collaboration:

· Collaborate across different teams to troubleshoot, test, and optimize various issues.

· Work seamlessly in a cross-functional environment.

Subject Matter Expert Support:

· Support sales, business development, product specialists, and associated departments as a subject matter expert.

Ad Hoc Tasks:

· Undertake other tasks as assigned based on project needs.

Flexible Work Schedules:

Adapt work schedules as needed to accommodate cell culture schedules.

Requirements

· Minimum Master’s degree in Biology or related science.

· At least 1-2 years related laboratory experience in mammalian cell culture, stem cells, immunology or exosomes.

· Experience with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) will be an advantage.

· Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).

· Experience in isolation of stem cells, tissue banking and generation of cell bank.

· Experience with cell assays such as FACS, ELISA, biological assays.

· Experience with bioreactor systems.

· General laboratory skills, good pipetting skills and experience with automation.

· Strong computer, scientific, and organizational skills.

· Excellent communication (oral and written) and attention to detail.

· Strong team player, develop positive relationship with a strong set of interpersonal skills.

· Ability to work independently and as part of a team, self-motivated, adaptable, and has a positive attitude.

· Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.

· Good presentation skills.

· A friendly and pleasant disposition.

Interested candidates, please submit a Cover Letter and CV to

Duties & Responsibilities

• Design and conduct experiments to address research objectives.
• Develop and optimize protein purification protocols to ensure high purity, yield, and activity.
• Execute and troubleshoot purification processes, including chromatography (affinity, ion exchange, size exclusion), filtration, and ultracentrifugation.
• Stay updated on scientific advancements through literature reviews.
• Perform laboratory work, including sample preparation, data collection, and analysis.
• Interpret results, draw conclusions, and present findings through reports and presentations.
• Collaborate with scientists, engineers, and cross-functional teams on research and product development.
• Maintain accurate experimental records in compliance with company policies and regulations.
• Assist in preparing research proposals, grant applications, and publications.
• Participate in scientific conferences, seminars, and workshops.

Requirements

Education:

• Bachelor's degree or higher in Biology, Chemistry, Biochemistry, Molecular Biology, or related fields.

Experience:

• 3-8 years of research experience in academia or industry, with a strong track record of scientific innovation.
• Experience in upscaling to production is a plus.

Technical Expertise:

• Proficiency in protein purification, cell culture, and relevant laboratory techniques.
• Strong knowledge of experimental design, data analysis, and statistical tools.
• Hands-on experience with purification techniques, including chromatography (affinity, ion exchange, size exclusion), filtration, and ultracentrifugation.

Skills & Competencies:

• Strong problem-solving skills, attention to detail, and ability to work independently and collaboratively.
• Excellent communication, presentation, and interpersonal skills.
• Familiarity with regulatory requirements and quality standards in scientific research.

Key Responsibilities:

• Develop both ELISA and Point-of-care test (POCT) kits immuno-based diagnostics kits for bladder cancer following the objectives and timelines in the T-Up program
• Define immunoassay format, technical specifications, parameters, and characteristics leading to prototyping
• Perform verification studies on optimised immunoassay using pre-pilot production
• Play a key role in design input and product requirements
• Contribute actively to quality activities relating to ISO 13485 such as risk management process, Failure Modes and Effects Analysis implementations (FMEA), traceability matrix, drafting of technical specification documentation and project planning
• Lead in diagnostic software development efforts including preparation of documents relating to software development such as Software System Requirements Document (SSRD), Software Architectural Design (SAD), Software Requirement Traceability Matrix (SRTM), Software Detailed Design (SDD) Software Hazard Analysis (SHA), and Software Development Plan (SDP)
• Conduct validation studies using clinical samples on design freeze prototype
• Close collaboration with scientists and other stakeholders to accelerate the productization of BioCheetah’s IVD products.

Minimum Qualifications:

• A Bachelor’s or a Master’s degree in Molecular Biology, Biotechnology, Life Sciences or related discipline
• A minimum of 5 years’ experience in R&D work

Experience and Skills:

• Strong proficiency in antibody usage in immunoassays with techniques in ELISA, western blot and dot blot
• Experience in immunoassay development for diagnostic purposes
• Prior experience in usage of clinical samples for immunoassay work
• Good foundation in molecular biology techniques eg. DNA cloning and RT-PCR
• Experienced in mammalian suspension cell culture and general tissue culture techniques
• Strong knowledge in experimental data analysis and experience in usage of analytical software such as GraphPad Prism or Microsoft Excel
• Experience in technical specification writing for immunoassay products
• Strong skills in problem-solving, communication, planning, documentation and organization
• Ability to work with little supervision
• Ability to pay keen attention to detail at all times
• Must be able to work within stipulated timeframes or deadlines even in the face of multiple responsibilities or projects
• Must be a team player
• Must exhibit a great level of self-discipline
• Proficient user of basic computer applications for the execution of daily project operations

About SUTD

SUTD is the world’s first Design AI university. With Design AI, artificial intelligence is treated as a partner and a member of the team – not just a tool. As a result of this unique SUTD treatment, AI and humans brainstorm, spar and prototype together, resulting in solutions that are elevated several-fold. This human-AI team concept has been made possible because of SUTD’s unique cohort-based interdisciplinary pedagogy. As a trailblazer in the field of design and technology education and research, SUTD has been pioneering innovative programmes and initiatives since its formation 16 years ago. As part its new mid-term growth strategy called SUTD Leap, it will work closely with industry to co-create solutions in both education and research – for a better world.

Job Description

The Research Assistant will be responsible for integrating the NeuroRAN AI-enabled Radio Access Networks (RAN) with various AI-based applications. Such applications will help optimize the RAN performance, streamline the RAN operational efficiency, create advanced features (e.g., spectrum sensing) for RAN, and better support edge-based AI applications.

Job Requirements:

• Bachelor or Master degree in computer science, computer engineering, communication engineering, or related fields.
• Good working knowledge in AI systems and models.
• Hands-on experiences in Linux systems, virtualization / containers, edge/cloud systems deployment and management (e.g., Kubernetes).
• Good programming skills, e.g.: Python, shell scripting, C / C++, Web, Java.
• Hands-on experience and working knowledge in developing and deploying networked systems and applications.
• Hands-on experience and working knowledge in deploying and operating wireless network (e.g., LTE, 5G networks) will be a plus.

Enabling Competencies:

• Analytical and problem-solving skills.
• Good interpersonal, communication and writing skills.
• Able to work independently and as a good team player.
• Adaptable and able to multi-task in a fast-paced environment.
• Ability to work under pressure.

Job Description

The Lee Kong Chian School of Medicine (LKCMedicine) trains doctors who put patients at the centre of their exemplary care. The School, which offers both undergraduate and graduate programmes, is named after local philanthropist Tan Sri Dato Lee Kong Chian. Established in 2010 by Nanyang Technological University, Singapore, in partnership with Imperial College London, LKCMedicine aims to be a model for innovative medical education and a centre for transformative research. The School’s primary clinical partner is the National Healthcare Group, a leader in public healthcare recognised for the quality of its medical expertise, facilities and teaching. The School is transitioning to an NTU medical school ahead of the 2028 successful conclusion of the NTU-Imperial partnership to set up a Joint Medical School. In August 2024, we welcomed our first intake of the NTU MBBS programme, that has been recently enhanced to include themes like precision medicine and Artificial Intelligence (AI) in healthcare, with an expanded scope in the medical humanities. Graduates from the five-year undergraduate medical degree programme will have a strong understanding of the scientific basis of medicine, with an emphasis on technology, data science and the humanities.

The school is inviting applications for a Research Assistant/Associate (RA) to support research and administrative tasks at Assistant Professor Michele Nguyen’s lab. The lab conducts data analytics to investigate extreme events in the healthcare setting, from adverse clinical outcomes to diseases outbreaks. With climate change and societal developments, the nature and impact of these events is changing. The research aims to produce evidence-based guidance to help society better prepare for and handle health extremes.

Key Responsibilities:

• Collate datasets and perform data analysis
• Read and critically evaluate existing literature on health extremes
• Contribute to the writing of progress reports and scientific papers
• Assist with day-to-day operations of the lab, including grants management and procurement

Key Competencies and Education Requirement:

• A Bachelor’s (for Assistant level) degree in fields such as Health Informatics, Data Science, Statistics, Public Health
• Experience in conducting literature reviews and data analysis
• Good written and oral communication skills
• Proficiency in statistical software (R) or other programming languages e.g. Python
• Experience with geospatial data is not a requirement but an advantage
• Willingness to learn new techniques and skills
• Self-motivated and well-organized with an eye for details
• Entry level candidates are welcome to apply

Job Details:

Location: Caldecott

Contract Duration: 1 year

Monday - Friday, office hours

Job Description:

To assist in research work for projects related to adult disability, social residential care, or early childhood industry. For this role, the main projects will involve the independent living assessment scale project, disability residential services review project, and research related to the family and adult support tool.

1. Conduct literature review

2. Collect data and manage database

3. Data collection involves conducting surveys/interviews with persons with disability (PwDs), caregivers, and social service staff

4. Analyse data and report findings

5. Provide administrative support

Requirements:

• Bachelor’s degree in Psychology or related social science discipline or candidates with relevant experience may apply
• Experience in quantitative research (e.g., thesis using quantitative methods)
• Experience or interest in working with PwDs or social services
• Willing to occasionally work after office hours or on weekends for data collection
• Knowledge in R or Python is a plus
• Knowledge in Tableau or Power BI is a plus
• Strong analytical and critical thinking skills

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MAJOR DUTIES AND RESPONSIBILITIES

(A) SPECIFIC (90%)

1. Liaison person with Principal Investigator (PI) and site-PI.
2. Liaison person with various departments for clinical research procedures e.g. Specialist Clinics, Laboratory, wards, etc.
3. Adherence to protocol procedure.
4. Screening and recruiting suitable candidates as research participants.
5. Explain protocol to research participants and ensure that informed consent is taken as per International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Guideline for Good Clinical Practice (GCP) and Human Biomedical Research Act (HBRA) requirements
6. Contact and schedule appointments for research subjects within the time frame required in the protocol.
7. Centrifuge blood specimens and send specimens to laboratory.
8. Tracing and returning of case notes, blood results and all other results required in the protocol.
9. Responsible for data collection and performing research procedures.
10. Maintain documentation of patient reimbursement logs, hardcopy and electronic case report forms.
11. Maintain source documentation for each patient accordance to protocol requirements.
12. Identify, document and submit protocol deviations to Institutional Review Board (IRB) according to hospital and sponsor procedures.
13. Inform PIs and collaborators on any adjustments based on protocol change.
14. Complete, report and follow up on unanticipated problems involving risk to subjects and adverse events and/or serious adverse events
15. Work with in-house Research Database IT Specialist on extraction of patient medical records and data mining.
16. Traveling to research participants’ house may be required.

(B) GENERAL (10%)

1. To participate in projects and activities as assigned by Director, Clinical Research Unit

JOB REQUIREMENTS

(A) EDUCATION, TRAINING AND EXPERIENCE

• Minimum Diploma in Biomedical Science or equivalent
• Experience as a Research Assistant will be preferred

If you like to express your interest or need further information about our job openings, please don’t hesitate to get in touch with us at

JOB SCOPE

Working in our analytics and research operations team, this entry-level role will support and be involved in the end-to-end process of market research, particularly in the area of qualitative research. The key areas include but are not limited to the following:

Research, Analysis and Insights

• Assist in designing and executing qualitative research projects, including focus groups, in-depth interviews, and ethnographic studies.
• Conduct secondary research to support project objectives.
• Help develop screeners, discussion guides, and interview scripts.
• Take notes and assist in moderating qualitative research sessions.
• Analyse qualitative data, identifying key themes and insights.
• Contribute to report writing, including summarizing findings and preparing presentations.
• Collaborate with senior researchers and clients to ensure high-quality research outcomes.
• Where applicable and required, integrate qualitative and quantitative (e.g. surveys and secondary data sources) research methodologies and findings.

Project Management

• Manage or assist in project setup and fieldwork management such as scheduling interviews, recruiting participants, arranging venues, and coordinating with vendors.
• Manage project timelines and collaborate with cross-functional stakeholders (i.e. client relations, operations, vendors, data science, etc.) to ensure timely project completion.
• Provide regular project or fieldwork updates to clients.

JOB REQUIREMENTS & EXPECTATION

• Bachelor’s degree in related field, such as market research, business, or marketing.
• 1-2 years of related work/internship experience is advantageous but otherwise fresh graduates are also welcomed.
• Strong attention to detail and able to multi-task with good time management.
• Possesses great soft skills and personality – approachable, candid, go-getting, and collaborative.
• Strong communication skills and the ability to work effectively with cross-functional teams.
• Ability to work independently and as part of a team in a fast-paced, deadline-driven environment.
• Exudes critical thinking and problem-solving skills to help mitigate problems and issues in projects.
• Proficient in Microsoft Excel, Word, and PowerPoint.
• Familiarity with dashboard solutions such as Tableau or PowerBI will be advantageous.
• Only applicants with eligibility to work in Singapore can be considered.

ABOUT US

Welcome to the Insights Table. We are a market research agency that sees ourselves being able to do better for the industry. On our table, we are proud of our drive, conviction, and authenticity to deliver best-in-class insights and value to our clients. We strive to create a work environment that excites and motivates our people on the table. An environment where individuals can be excited about starting their day, with a purpose, every day. This is a table where insights are uncovered, curiosity leads to answers, important agendas are discussed, and informed decisions are made. Above all, everyone on the table enjoys coming together.

Research Scientist, Pharmacology - Hummingbird Bioscience

Full time position – Singapore-based location

ABOUT HUMMINGBIRD BIOSCIENCE

Hummingbird Bioscience is a biotherapeutics company working at the interface of artificial intelligence and human innovation to discover and develop transformative medicines for hard-to-treat diseases. Hummingbird Bioscience’s computational and systems biology technologies have generated a pipeline of innovative clinical-stage monoclonal antibodies and antibody-drug conjugates in oncology and autoimmunity. At Hummingbird Bioscience, the commitment to rigorous science, teamwork, and intellectual integrity underpins our passion to accelerate the journey of new drugs from concept to clinic.

For more information, please visit , and follow Hummingbird Bioscience on LinkedIn , X (formerly Twitter) , and YouTube .

About the role

Hummingbird Bioscience is seeking a Research Scientist – Preclinical pharmacology to support the Pharmacology team. This will be a permanent role for the right candidate with ample opportunity to learn, grow and contribute to innovative drug development projects. The ideal candidate is a highly organized and proactive individual with a background in life sciences and a collaborative mindset who thrives in a fast-paced biotech environment.

Key responsibilities

• Coordinate the execution of in vitro and in vivo preclinical studies by interfacing with internal scientific teams and external CROs; ensure alignment on study design, timelines, logistics, and data collection to support key development milestones
• Support study start-up and execution by reviewing and organizing study plans, protocols, contracts and communication workflows
• Manage procurement, shipment, and inventory processes for reagents, samples, and study-related materials
• Perform literature review, data analysis and support preparation of reports, presentations, and dashboards to aid project tracking and decision-making

Essential qualifications

• PhD in a scientific discipline such as biology, biomedical sciences or a related field
• At least 1–2 years of hands-on experience managing preclinical research projects, preferably in cancer biology and immunology, within biotech, pharma, or academic settings
• Proficiency in MS office and data analysis tools such as GraphPad
• Prior experience of working in a CRO environment
• Strong communication and interpersonal skills, with proficiency in English and Mandarin to facilitate effective collaboration with external stakeholders and CROs, including those based in China

Desirable qualifications

• Background or experience working with therapeutic antibodies and or antibody-drug conjugates

OUR MISSION & VALUES

Our fast-growing biotechnology company is committed to discovering and developing important new drugs for cancer and autoimmune diseases, and living by our values: Excellence, Determination, Teamwork, Intellectual Integrity and Audacity.

JOIN US AT THE FRONTIER OF DRUG DISCOVERY AND DEVELOPMENT

We are looking for passionate and motivated individuals committed to solving important, complex problems. We are committed to the personal and professional development of our team and offer robust learning and development programs. Hummingbird Bioscience understands the need for flexibility for our team and offers a generous paid time off program with flexibility to support employees through different life stages. We invest in our team’s health by offering competitive benefits including health and dental insurance, and a comprehensive and holistic employee assistance program. We foster a more collaborative, productive, and sociable culture with on-site lunches and snacks. Finally, we believe in creating social impact beyond our business through corporate social responsibility initiatives.

Are you ready to join us on our mission to discover and develop important new drugs for cancer and autoimmune disease? Click on ‘Apply for this Job’ to submit your application.

For further enquiries, please email us at .

Hummingbird Bioscience is firmly committed to Equal Employment Opportunity (EEO) and to compliance with all Singapore and US federal, state and local laws and/or guidelines that prohibit employment discrimination on the basis of age, race, color, gender, sexual orientation, gender identity, ethnicity, national origin, citizenship, religion, genetic carrier status, disability, pregnancy, childbirth or related medical conditions, marital status, protected veteran status and other protected classifications.