1,226 Scientific Research & Development jobs in Singapore
Quality Assurance Specialist (Pharma/Biotech)
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Quality Assurance Specialist (Pharma/Biotech)
Overview
- Ensure adherence to the Change Control management systems and processes.
- Develop competency and proficiency in the QA Change Control process and the associated tools, supporting the delivery of training for change users as needed.
- Evaluate Change Control requests for process, validation, regulatory and product impact.
- Coordinate the review and approval process of change requests to ensure timely execution of changes.
- Ensure all site changes are managed appropriately to meet the expectation of the global change control board (if applicable) and meet site project timelines.
- Participate in cross functional and cross site change management forums.
- Collaborate with departments to ensure change control activities are executed efficiently and effectively, to provide supporting assistance to stakeholders in the process.
- Ensure completion of required change control actions prior to lifting lot disposition restrictions.
- Assist in the development and delivery of training materials and qualifications for Change Control processes and Change Management applications.
- Perform Change Records review in support of Annual Product Review activities.
- Ensure maintenance and continuous improvement of change control and processes.
- Support regulatory inspections and provide audit support with team, which may include presentations and facility, utility, equipment documentation review.
- Compliance with cGMP and site safety & security regulations at all times.
- Any other duties as assigned by supervisor or manager.
- Ensure adherence to the Change Control management systems and processes.
- Develop competency and proficiency in the QA Change Control process and the associated tools, supporting the delivery of training for change users as needed.
- Evaluate Change Control requests for process, validation, regulatory and product impact.
- Coordinate the review and approval process of change requests to ensure timely execution of changes.
- Ensure all site changes are managed appropriately to meet the expectation of the global change control board (if applicable) and meet site project timelines.
- Participate in cross functional and cross site change management forums.
- Collaborate with departments to ensure change control activities are executed efficiently and effectively, to provide supporting assistance to stakeholders in the process.
- Ensure completion of required change control actions prior to lifting lot disposition restrictions.
- Assist in the development and delivery of training materials and qualifications for Change Control processes and Change Management applications.
- Perform Change Records review in support of Annual Product Review activities.
- Ensure maintenance and continuous improvement of change control and processes.
- Support regulatory inspections and provide audit support with team, which may include presentations and facility, utility, equipment documentation review.
- Compliance with cGMP and site safety & security regulations at all times.
- Any other duties as assigned by supervisor or manager.
- Bachelor7s degree or higher in Biologics, Pharmacy, Pharmaceutical Engineering, Bioengineering, or other relevant fields.
- 3+ years of experience in a GMP-regulated biopharmaceutical or pharmaceutical manufacturing environment.
- Duration: 12-month contract role
- Seniority level: Mid-Senior level
- Employment type: Contract
- Job function: Quality Assurance
- Industries: Business Consulting and Services
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#J-18808-LjbffrLab Technician
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Job Title: Lab Technician
Location: Singapore
About Us:
The company is a leading cord blood and cord tissue banking company dedicated to “providing a choice of new medical care for new life.” In this role, you will play a vital part in the separation, processing, and storage of cord blood and umbilical cord samples, contributing to the advancement of regenerative medicine.
Key Responsibilities:
Assist in the separation, processing, and storage of cord blood and umbilical cord samples according to established protocols
Adhere strictly to Standard Operating Procedures (SOPs) to ensure the proper and safe handling of all biological specimens
Ensure proper labeling and tracking of specimens at all stages of processing to maintain chain of custody
Maintain a clean, organized, and contamination-free work environment, following all established hygiene standards
Qualifications:
Bachelor's degree in Life Sciences, Biotechnology, or a related scientific field
3-5 years of experience in hands-on experience working in a laboratory setting, specifically with biological sample processing.
Solid understanding of basic laboratory techniques and safety protocols
Ability to work both independently and collaboratively as part of a team
Interested applicant, please click APPLY NOW
Do note that we will only be in touch if your application is shortlisted.
Peh Yong Sin
JAC Recruitment Pte Ltd
EA License Number: 90C3026
EA Personnel: R
#LI-JACSG
#countrysingapore
#J-18808-LjbffrLab Scientist (Contractual)
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Lab Scientist (Contractual)
Date: Jul 28, 2025
Location: Singapore, SG,
Company: Corning
Role Purpose:
Designs, executes, and analyzes experiments to help in developing new products and processes and optimize existing process. Uses scientific methods to design, analyze and report on experiments to solve difficult technical problems or enhance fundamental understanding. Serves as a technical expert in field. The Singapore lab scientist will also support for providing resolutions/answer to scientific queries from both customers and internal/ channels sales reps.
Key Responsibilities:
Serves as a technical expert in upstream processing.
Manages equipment and resources to keep lab running in good working order.
Should have a scientific acumen to troubleshoot the experimental issues.
Documents data and writes reports and Standard Operating Procedures (SOPs) for laboratory processes and instrumentation.
Holds technical trainings to customer, distributors, and internal sales reps.
Functions as a team member on focused projects.
Trains or coaches’ new employees, technicians, and interns, on laboratory processes, equipment, and instrumentation.
Supports and/or leads continuous improvement activities on products, processes, and cost reduction projects.
Presents and/or speaks with end users on technical specifications of the product during lab tour.
Provide scientific resolution to queries received from customer or channel partners.
Abide all the safe GLP practices.
Experiences/Education:
Minimum of master’s degree in the life sciences
Ph.D. (or equivalent research experience) in life sciences desired
Strong and solid fundamental knowledge of life sciences, hands on experience on Bioprocess, cell biology and molecular biology is must.
3+ years of mammalian cell culture experience, preferably from industry.
2+ years of bioprocessing experience for large-scale cell production using bioreactors.
Demonstrated ability to solve complex technical issues
Multilingual with Thai language preferred (proficient in English).
Familiarity with lab equipment.
Desired Skills
Experience with vaccine and/or viral vectors (AAV, AV, LV) productions.
Familiarity with stem cell and/or immune cell workflows.
Understanding of culture conditions for common bioproduction
cell lines (HEK293, Vero).
Handling of stacked vessel technologies, including Cell STACK and Hyperstack.
Knowledgeable of Fixed-Bed Bioreactors or Rocker Bioreactors.
Ability to meet deadlines independently with minimal direction.
Flexibility in schedule to complete projects, tasks, and goals.
Experience with cell line development.
Performance Metrics:
Meet project milestones and deliverables.
Number of scientific queries resolution.
Quantified commercial/cost savings over time.
Lab and individual safety record.
Soft Skills:
Flexibility in schedule and be able to travel within assigned regions.
Excellent written, verbal, and presentation skills.
Ability to function in a multi-tasking environment.
Proven problem-solving skills.
Great teammate.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, disability status or any other legally protected status.
#J-18808-LjbffrLaboratory Analyst
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Clinical Research Coordinator
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National Cancer Centre of Singapore Pte Ltd
Clinical Research CoordinatorJob Category: Research
Posting Date: 15 Jan 2025
As a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance with the ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.
You will support and assist the Principal Investigator in the following trial-related activities:
- Patient screening and recruitment
- Monitoring subject’s compliance to their treatment and follow-up
- Data collection and management including resolving data discrepancies
- Coordinating the collection of biological specimens
- Monitoring of adverse events and safety reporting
- Maintaining and organizing investigator site files, preparation and submissions to the ethics committee and relevant local health authorities
- Tracking trial expenditures and timely invoicing
Requirements:
- Degree in Life Sciences/ Nursing/ Biomedical Science/ Biological Sciences
- 1-2 years of related working experience will be advantageous
- Good time-management and strong ability to multi-task
- Able to work independently and as a team
- Conscientious, meticulous, and self-motivated
Lead Scientist (Cell Line Creation)
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Join us for the world we are making, redefining biosolutions for current and future generations to come, transcending planetary boundaries, sustainability, and One Health.
The OpportunityEsco 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.
Who we’re looking for- 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 or review standard operating procedures and other related documents.
- Ability to define problems, collect data, establish facts, and draw conclusions.
- Ability to focus.
- Repetitive motions due to certain laboratory techniques.
You will be part of Esco Aster’s Cell Line Creation division and contribute to the company’s CDMO mission and objectives. You will plan and execute experiments in support of the cell line generation division and generate high productivity mammalian cell lines and execute the diverse cell culture experiments required to produce various vaccine candidates and antibodies, in collaboration with internal and external stakeholders, clients and partners.
Primary work location: Ayer Rajah, Singapore.
Reports to: Head of Scientific & Sales Operations.
Job Responsibilities- Perform key activities associated with cell line development including molecular cloning, in vitro transcription, transfection, Single cell cloning, clone selection, characterization and cell banking.
- Perform tasks in a compliant manner according to SOP guidelines and regulations.
- Write technical reports and campaign summaries.
- Prepare solutions and culture media (small scale as well as large scale).
- Perform analysis of cell metabolites, medium components etc. by Bioanalysis.
- Maintain accurate batch records and results following good manufacturing practices (GMP).
- Work independently and efficiently.
- Document work clearly and perform tests accurately.
- Communicate effectively with client staff members and provide updates on the progress of the project.
- Liaise with vendors and third-party testing labs to procure materials and obtain test results in a timely manner.
- At least 1-2 years related laboratory experience including aseptic and mammalian cell culture techniques.
- Microbiology/Cell biology Background.
- Experience with bioreactor systems.
- Good troubleshooting ability with cell lines.
- General laboratory skills, good pipetting skills and experience with automation.
- Experience using formulas and linking spreadsheets in Excel.
- Strong computer, scientific, and organizational skills.
- Excellent communication (oral and written) and attention to detail.
- Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
- Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
- A friendly and pleasant disposition.
- Masters in Biology or related science and 1-2 Years Mammalian Cell Culture experience.
Clinical Research Coordinator
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National Neuroscience Institute of Singapore
Clinical Research CoordinatorJob Category: Research
Posting Date: 11 Jan 2025
We are looking for a candidate who will be providing research support service to the investigators in the conducting and implementation of clinical trial and/or clinical research studies at the National Neuroscience Institute (TTSH campus), in adherence to Singapore Guideline for Good Clinical Practice (SGGCP) and protocol requirements.
There will be opportunities to:
- Contribute to clinical trials set-up, feasibility and coordination
- Contribute to data processing and analysis of results for multiple studies conducted within the department
- Acquire new skillsets, such as imaging handling, processing and analysis
- Gain experience in scientific writing for presentations and publications
Requirements:
- Bachelor’s degree in Life Sciences, Psychology or related fields
- Good communications and interpersonal skills
- Good IT literacy and statistics skills are also desirable
- Prior experience in a clinical environment and/or with clinical trials/studies would be most advantageous
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Research Fellow (Mechanobiology Institute)
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Overview
The Mechanobiology Institute (MBI) at the National University of Singapore (NUS) is a leading multi-disciplinary institute devoted to developing new paradigms for understanding biological functions in health and diseases from the perspective of cell, tissue and organ mechanics/dynamics and mechano-signal transduction. The institute operates on a fully integrated open-lab philosophy, with an extensive infrastructure supported by core facilities dedicated to technology such as state-of-the-art light microscopy, nano- and micro-fabrication, and computing.
PositionResearch Fellow (Mechanobiology Institute) within the lab of Prof. Rong Li. The successful candidate will conduct cutting-edge research in the fields of cell therapy and cell rejuvenation, with a focus on improving the fitness of reproductive cells. Responsibilities include designing and executing experiments, analyzing data, preparing manuscripts, and presenting findings at scientific meetings. The candidate will also have opportunities to collaborate with interdisciplinary teams within the MBI and across the world.
Responsibilities- Design and execute experiments related to cell therapy and cell rejuvenation with a focus on improving the fitness of reproductive cells.
- Analyze data and prepare manuscripts for publication; present findings at scientific meetings.
- Collaborate with interdisciplinary teams within the Mechanobiology Institute and with external partners.
- PhD in Cell Biology, Molecular Biology, Developmental Biology, or a closely related field
- Demonstrated expertise in stem cell biology, including experience with induced pluripotent stem cell (iPSC) differentiation, or a strong background in advanced mammalian cell culture techniques
- Proven ability to work independently and as part of a collaborative team
- Excellent written and oral communication skills
- An interest in joining a future startup is desired
The position is available immediately and will remain open until filled. Interested applicants should include the following with their online application:
- a cover letter describing their research experience and interests
- their Curriculum Vitae
- the contact information for at least two academic referees
For more information about the Mechanobiology Institute, please visit:
We regret that only shortlisted candidates will be notified.
More Information- Location: Kent Ridge Campus
- Organization: Mechanobiology Institute
- Department: Research
- Employee Referral Eligible: No
- Job requisition ID: 28713
Associate Clinical Research Coordinator, Ophthalmology
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Associate Clinical Research Coordinator, Ophthalmology
The Clinical Research Coordinator (CRC) will work closely with the Principal Investigator (PI), study team members, Research Director, Research Manager and supporting teams to ensure the successful planning, execution, and completion of clinical trials and research projects. The CRC will play a key role in participant recruitment, data management, and regulatory compliance, contributing to impactful clinical research.
Job Responsibilities- Plan, coordinate, and execute clinical research studies from initiation to close-out, ensuring adherence to study protocols and timelines.
- Screen, recruit, and enrol eligible study participants, obtaining informed consent in accordance with ethical and regulatory requirements.
- Collect, manage, and analyze study data in line with protocol requirements and regulatory standards, ensuring data integrity and accuracy.
- Maintain comprehensive and organized study documentation, including regulatory binders, case report forms, and participant records.
- Collaborate with study sponsors, regulatory authorities, and study sites to ensure ongoing compliance and efficient study progress.
- Manage study drug and device inventory, ensuring proper storage, handling, and accountability.
- Monitor and report adverse events, protocol deviations, and other critical issues to study sponsors and regulatory authorities as required.
- Assist in the preparation and submission of study progress reports, regulatory submissions, and ethics applications.
- Ensure full compliance with Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements.
- Support the Research Manager in grant planning, budget verification, cost assessments, monthly invoicing, and account management.
- Contribute to department events, ad-hoc projects, and other administrative duties as needed.
- Registered Optometrist with Singapore Optometrists & Opticians Board (OOB).
- Have diploma and/or first degree with good results; preferably with some experience in research.
- Candidates with a basic understanding of statistical analysis are preferred.
- Able to work independently and in a team, with an investigative nature and attention to detail.
- Have knowledge of computer applications, e.g. SPSS, MS Office, PowerPoint.
- Prior experience in clinical research or healthcare is advantageous.
- Strong organizational skills and attention to detail.
- Effective communication and interpersonal skills for engaging with study participants, team members, and external collaborators.
- Familiarity with GCP, clinical trial processes, and relevant regulatory standards.
- Entry level
- Contract
- Research, Science, and Administrative
- Hospitals and Health Care, Research Services, and Hospitals
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#J-18808-LjbffrData Scientist
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As a Data Scientist (Genomics), you will be responsible for the following duties:
- Conduct comprehensive data analyses using a range of machine learning algorithms and statistical techniques.
- Apply deep learning methods to integrate multi-omics data with radiomic features derived from CT and X-ray imaging.
- Extract meaningful insights from complex datasets and present findings in a clear, structured manner to support scientific content development.
- Utilize data analysis to identify novel DNA, RNA, or non-coding RNA biomarkers for cancer, or to develop predictive models for multi-marker diagnostic tests.
- Design and implement innovative analytical tools and methodologies to enhance data interpretation, improve data generation processes, and ensure quality control.
- Provide statistical expertise in experimental design, process optimization, and the development of quality control protocols.
- Contribute analytical support to various commercial and cross-functional initiatives.
- Any other ad hoc duties as assigned.
Requirements:
- Possess a PhD/MSc. in related science background
To apply, simply click on the “apply” button in the job advertisement or alternatively, you can send in your resume via email:
We regret to inform that only shortlisted candidates will be notified.
ALLIED SEARCH PTE. LTD.
EA LICENSE : 19C9777
Seniority level- Mid-Senior level
- Full-time
- Research and Health Care Provider
- Industries: Biotechnology Research, Medical Practices, and Hospitals and Health Care