106 Formulation Scientist jobs in Singapore

• Develop new products according to development requests and improve existing products.
• Develop application recipes to optimize product design for new and existing products.
• Monitor new trends and products in the market.
• Evaluate new ingredient submissions.
• Conduct food tasting and sensory evaluations.
• Maintain proper documentation to support costing, lab-scale formulation of new and existing products, and any supporting documents.
• Work closely with inter-departments on the development and launch of new or improved recipes.
• Perform ad-hoc duties assigned by immediate superior.

Job Requirements

• Recognized culinary qualification or similar discipline.
• At least 2 - 5 years of relevant experience in the restaurant, hotel business, or food manufacturing industry.
• Experience in different Asian cuisines, bakery, and Dim Sum would be beneficial for daily R&D work.
• Creative in food preparation and presentation.
• Meticulous with good organizational skills.
• Team player with good interpersonal skills.
• Proficient with Microsoft Office.
• Proficient in Mandarin and English (spoken and written) as daily liaison with Mandarin and English speaking associates is required.

Tee Yih Jia Food Manufacturing Pte Ltd is the leading frozen foods manufacturer in Singapore, exporting more than 90% of our renowned Spring Home products to countries such as Europe, North America, South Africa, the Middle East, and Asia Pacific. Tee Yih Jia has world-class manufacturing facilities in Singapore, Malaysia, China, and the United States, which hold international certifications of quality controls and hygiene such as HACCP and BRC.

Join to apply for the Research Development Manager role at National University of Singapore .

Support the Vice Dean and Assistant Deans in the Office of Research and Technology (ORT) to grow research within the College of Design and Engineering (CDE) and NUS:

• Lead in studying research trends and funding landscape, identifying potential funding opportunities for CDE under the Research, Innovation and Enterprise (RIE) framework.
• Formulate and implement strategies to drive growth by securing funding aligned with CDE’s goals.
• Analyze historical CDE funding data to assess research capabilities, identifying strengths and gaps.
• Develop recommendations for future funding strategies and compile comprehensive reports to enhance research capabilities and growth.
• Spearhead collaborative efforts, leading the development, execution, and management of high-impact research strategies and large-scale programmes, ensuring timely delivery within scope.
• Monitor and assess the impact of strategies and programmes, refining them based on effectiveness and alignment with ORT goals, and drive corrective actions as needed.
• Draft ad-hoc research-related reports and presentations.
• Undertake additional initiatives as directed by the Vice Dean (Research and Technology), demonstrating ability to align initiatives with broader objectives.

Qualifications

• Recognised honours degree in a STEM discipline.
• At least 5 years of experience in research management.
• Self-starter with initiative to work in a fast-changing environment.
• Good communication skills, outgoing personality, and a team player.
• Strong analytical and project management skills.
• Good understanding of the local research, innovation, and enterprise ecosystem.
• Resourceful and problem-solver.

Seniority level

Not Applicable

Employment type

Full-time

Job function

Public Relations, Research, and Education

Industries

Higher Education, Research Services, and Non-profit Organizations

Health Services Research Specialist

This is a challenging role for a highly motivated and skilled individual who can lead research initiatives in healthcare services. The position holder will be responsible for formulating health services research ideas, working with healthcare professionals, applying for funding, and guiding junior researchers.

Primary Responsibilities:

• Work on projects related to health services and operational research.
• Write and review research papers, present research outcomes, and develop collaborations.
• Contribute to project management and provide guidance to other healthcare worker researchers.

Secondary Duties:

• Develop own portfolio of research work and projects.
• Work with PI(s) perform research grant administrative matters such as variation & extension requests, submission of claims and progress reports etc.
• Assume additional responsibilities as assigned by reporting officer/HOD.

Requirements:

• PhD/Master/Degree in Nursing/Medicine or related discipline.
• 4-5 years of experience in medical research is a plus.
• Expertise in health services research (HSR) and applied statistics, with experience in study design, data analysis, and outcome evaluation.
• Strong background in developing and implementing data-driven solutions for healthcare improvement, with proficiency in AI methodologies (e.g., machine learning, predictive modelling) where applicable.
• Proven ability to independently manage and execute projects across diverse health services domains, from conceptualization through to implementation, including data collection, analysis, and interpretation.
• Proficiency in programming languages such as Python or R, with experience in using machine learning and analytical frameworks to solve healthcare-related problems.

What We Are Looking For:

• A strong track record of achievement in health services research and related fields.
• The ability to work collaboratively with multidisciplinary teams.
• Excellent communication and interpersonal skills.
• The ability to think creatively and outside the box.
• A high level of organisational and time management skills.

Contact Us:

If you are interested in this opportunity, please contact us to discuss further.

We are seeking a skilled Research Development Specialist to support the daily operations of our clinical trial facility. The ideal candidate will have experience in research settings, outpatient care, or preventive health clinics.

• Assist with participant check-in, preparation, and monitoring during study visits and interventions.
• Perform clinical tasks such as vital signs measurement, phlebotomy, sample handling, and documentation under study protocol.
• Support lifestyle and physical assessments, including gait analysis, grip strength, and other functional tests.
• Provide assistance in managing incidental findings and ensure proper escalation to the Clinical Research Manager or PI.
• Maintain cleanliness, safety, and readiness of the clinical space and equipment.

• Bachelor's Degree
• Registered Nurse (RN) or equivalent qualification recognized in Singapore.
• Minimum of 1–2 years of clinical experience, preferably in research settings or preventive health clinics.
• Strong interpersonal and organizational skills.
• Comfortable working in a fast-paced, multidisciplinary environment.

This is an exciting opportunity for individuals who are passionate about contributing to the advancement of healthy longevity. If you are a team player with excellent communication skills and a strong work ethic, we encourage you to apply.

• Flexible scheduling to accommodate various shifts and weekend work may be required.
• Participation in on-the-job training and professional development opportunities.

The ideal candidate will have a strong background in control engineering, mechatronics, or a related field.

• Key Responsibilities:
• Conduct research and development
• Assemble components
• Design and implement control systems
• Manage projects from inception to completion

• Requirements:
• Education: Master's degree in Control Engineering, Mechatronics, or a related field
• Skills: Proficient in control system design, hardware integration, Matlab, Python, Arduino
• Experience: Minimum 2 years of relevant research experience
• Competencies: Strong problem-solving skills, attention to detail, initiative, and commitment to delivering high-quality research outcomes

Job Responsibilities
Develop new products according to development requests and improve existing products.
Develop application recipes to optimize product design for new and existing products.
Monitor new trends and products in the market.
Evaluate new ingredient submissions.
Conduct food tasting and sensory evaluations.
Maintain proper documentation to support costing, lab-scale formulation of new and existing products, and any supporting documents.
Work closely with inter-departments on the development and launch of new or improved recipes.
Perform ad-hoc duties assigned by immediate superior.
Job Requirements
Recognized culinary qualification or similar discipline.
At least 2 - 5 years of relevant experience in the restaurant, hotel business, or food manufacturing industry.
Experience in different Asian cuisines, bakery, and Dim Sum would be beneficial for daily R&D work.
Creative in food preparation and presentation.
Meticulous with good organizational skills.
Team player with good interpersonal skills.
Proficient with Microsoft Office.
Proficient in Mandarin and English (spoken and written) as daily liaison with Mandarin and English speaking associates is required.
Tee Yih Jia Food Manufacturing Pte Ltd
is the leading frozen foods manufacturer in Singapore, exporting more than 90% of our renowned Spring Home products to countries such as Europe, North America, South Africa, the Middle East, and Asia Pacific. Tee Yih Jia has world-class manufacturing facilities in Singapore, Malaysia, China, and the United States, which hold international certifications of quality controls and hygiene such as HACCP and BRC.
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Associate Scientist/Scientist, LNP Formulation & Process Development

Posting Date : 18 Aug 2025 | Closing Date :17 Oct 2025

Job Title: Associate Scientist/Scientist, LNP Formulation & Process Development

Organization: Platform Technology

Job Type: Full Time

About NATi:

The Nucleic Acid Therapeutics Initiative (NATi), hosted by A*STAR, is Singapore's national platform dedicated to advancing RNA-based medicines and revolutionizing drug and vaccine development. NATi's mission is to establish Singapore as a globally recognized hub of excellence in nucleic acid therapeutics research, clinical translation, and commercialization.

NATi focuses on key RNA modalities such as antisense oligonucleotides (ASOs), small interfering RNA (siRNA), and messenger RNA (mRNA). To drive this vision, NATi is building a biotech-like translational engine focused on asset and technology development spanning discovery to clinical development.

We are actively seeking passionate and committed RNA scientists with deep translational expertise to join us in advancing the next generation of RNA-based therapeutics.

Position Overview

The Associate Scientist/Scientist , LNP Process Development will lead the formulation and process development of lipid nanoparticles (LNPs) for RNA delivery across multiple therapeutic programs. This role is central to NATi's translational strategy, enabling robust and scalable LNP process development and supporting clinical advancement via seamless technology transfer. The successful candidate will establish robust, scalable, and reproducible LNP manufacturing processes usingQuality by Design (QbD)principles, supporting production from early-stage research through preclinical and pilot-scale batches. The successful candidate will also drivetechnology transfer to external CDMOs, ensuring alignment with regulatory and quality standards for clinical development.

Key Responsibilities

Develop and optimize LNP formulation processes for different RNA payloads (e.g., mRNA, circRNA, saRNA, gRNA), focusing on encapsulation efficiency, particle size control, and stability.

Design and implement high-throughput, automated workflows for LNP formulation and purification, leveraging scalable technologies (e.g., microfluidics, TFF systems) to support rapid screening, process optimization, and multiscale production (mg to gram) from discovery through pilot-scale manufacturing.

ApplyQbD principlesto define critical process parameters (CPPs) and critical quality attributes (CQAs) for LNP manufacturing workflows.

Integrate process analytical technologies (PAT) for real-time monitoring and control of LNP manufacturing workflows.

Design and execute process development studies coupled with robust characterization workflows to support preclinical, toxicology, and pilot-scale manufacturing.

Collaborate with analytical teams to develop and validate methods for LNP characterization (e.g., DLS, encapsulation efficiency, TEM, HPLC).

Develop and maintain SOPs and batch records to ensure reproducibility, compliance, and readiness for GMP environments.

Maintain accurate records using LIMS/ELN systems to support data integrity and reproducibility.

Prepare technical reports, presentations, and documentation to support internal decision-making and external regulatory submissions.

Leadtech transfer activitiesto external CDMOs, including preparation of documentation, training, and troubleshooting support.

Support regulatory submissions by generating process development reports and contributing to CMC documentation.

Qualifications & Experience

MS or Ph.D. degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Material Engineering or a related field.

Minimum of 4+ (with a Ph.D. degree) or 7+ (with a MS degree) years of experience in LNP formulation and process development in pharmaceutical or biotech settings; Scientist candidates are expected to demonstrate leadership in cross-functional project teams, strategic input into platform development, and mentoring of junior staff.

Demonstrated hands-on experience in designing and implementing high-throughput, automated workflows for LNP formulation and purification, utilizing scalable technologies (e.g., microfluidics, TFF, sterile filtration) to support rapid screening, process optimization, and multiscale production.

Experience applying Quality by Design (QbD) principles in LNP process development, including the use of Design of Experiments (DoE), risk assessments (e.g., FMEA), and control strategies to define and optimize critical process parameters (CPPs) and critical quality attributes (CQAs) for scalable and reproducible manufacturing.

Proven track record of experience in regulatory filing for RNA-based therapeutics, IND-enabling CMC studies, and supporting documentation.

Experience in lyophilization process development for LNP-based formulations, including optimization of cryoprotectants, cycle design, and stability assessment is highly desirable.

A track record oftech transfer to CDMOs, including documentation and on-site support is a plus.

Strong problem-solving skills and ability to work independently and collaboratively in a fast-paced multidisciplinary environment.

Global Recruitment & Competitive Compensation

NATi is conducting a global search for top-tier talent in RNA therapeutics. We welcome applications from leading pharmaceuticals scientists and biotech innovators worldwide.

This role provides a highly competitive compensation package aligned with global industry standards, including attractive benefits and long-term career growth opportunities within Singapore's thriving biomedical innovation ecosystem. Join us in shaping the future of RNA-based medicines and establishing Singapore as a world-class hub for nucleic acid therapeutics.

The above eligibility criteria are not exhaustive. A*STAR may include additional selection criteria based on its prevailing recruitment policies. These policies may be amended from time to time without notice. We regret that only shortlisted candidates will be notified.

Associate Scientist/Scientist, LNP Formulation & Process Development

Posting Date : 18 Aug 2025 | Closing Date :17 Oct 2025

Job Title: Associate Scientist/Scientist, LNP Formulation & Process Development

Organization: Platform Technology

Job Type: Full Time

About NATi:

The Nucleic Acid Therapeutics Initiative (NATi), hosted by A*STAR, is Singapore's national platform dedicated to advancing RNA-based medicines and revolutionizing drug and vaccine development. NATi's mission is to establish Singapore as a globally recognized hub of excellence in nucleic acid therapeutics research, clinical translation, and commercialization.

NATi focuses on key RNA modalities such as antisense oligonucleotides (ASOs), small interfering RNA (siRNA), and messenger RNA (mRNA). To drive this vision, NATi is building a biotech-like translational engine focused on asset and technology development spanning discovery to clinical development.

We are actively seeking passionate and committed RNA scientists with deep translational expertise to join us in advancing the next generation of RNA-based therapeutics.

Position Overview

The Associate Scientist/Scientist , LNP Process Development will lead the formulation and process development of lipid nanoparticles (LNPs) for RNA delivery across multiple therapeutic programs. This role is central to NATi's translational strategy, enabling robust and scalable LNP process development and supporting clinical advancement via seamless technology transfer. The successful candidate will establish robust, scalable, and reproducible LNP manufacturing processes usingQuality by Design (QbD)principles, supporting production from early-stage research through preclinical and pilot-scale batches. The successful candidate will also drivetechnology transfer to external CDMOs, ensuring alignment with regulatory and quality standards for clinical development.

Key Responsibilities

Develop and optimize LNP formulation processes for different RNA payloads (e.g., mRNA, circRNA, saRNA, gRNA), focusing on encapsulation efficiency, particle size control, and stability.

Design and implement high-throughput, automated workflows for LNP formulation and purification, leveraging scalable technologies (e.g., microfluidics, TFF systems) to support rapid screening, process optimization, and multiscale production (mg to gram) from discovery through pilot-scale manufacturing.

ApplyQbD principlesto define critical process parameters (CPPs) and critical quality attributes (CQAs) for LNP manufacturing workflows.

Integrate process analytical technologies (PAT) for real-time monitoring and control of LNP manufacturing workflows.

Design and execute process development studies coupled with robust characterization workflows to support preclinical, toxicology, and pilot-scale manufacturing.

Collaborate with analytical teams to develop and validate methods for LNP characterization (e.g., DLS, encapsulation efficiency, TEM, HPLC).

Develop and maintain SOPs and batch records to ensure reproducibility, compliance, and readiness for GMP environments.

Maintain accurate records using LIMS/ELN systems to support data integrity and reproducibility.

Prepare technical reports, presentations, and documentation to support internal decision-making and external regulatory submissions.

Leadtech transfer activitiesto external CDMOs, including preparation of documentation, training, and troubleshooting support.

Support regulatory submissions by generating process development reports and contributing to CMC documentation.

Qualifications & Experience

MS or Ph.D. degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Material Engineering or a related field.

Minimum of 4+ (with a Ph.D. degree) or 7+ (with a MS degree) years of experience in LNP formulation and process development in pharmaceutical or biotech settings; Scientist candidates are expected to demonstrate leadership in cross-functional project teams, strategic input into platform development, and mentoring of junior staff.

Demonstrated hands-on experience in designing and implementing high-throughput, automated workflows for LNP formulation and purification, utilizing scalable technologies (e.g., microfluidics, TFF, sterile filtration) to support rapid screening, process optimization, and multiscale production.

Experience applying Quality by Design (QbD) principles in LNP process development, including the use of Design of Experiments (DoE), risk assessments (e.g., FMEA), and control strategies to define and optimize critical process parameters (CPPs) and critical quality attributes (CQAs) for scalable and reproducible manufacturing.

Proven track record of experience in regulatory filing for RNA-based therapeutics, IND-enabling CMC studies, and supporting documentation.

Experience in lyophilization process development for LNP-based formulations, including optimization of cryoprotectants, cycle design, and stability assessment is highly desirable.

A track record oftech transfer to CDMOs, including documentation and on-site support is a plus.

Strong problem-solving skills and ability to work independently and collaboratively in a fast-paced multidisciplinary environment.

Global Recruitment & Competitive Compensation

NATi is conducting a global search for top-tier talent in RNA therapeutics. We welcome applications from leading pharmaceuticals scientists and biotech innovators worldwide.

This role provides a highly competitive compensation package aligned with global industry standards, including attractive benefits and long-term career growth opportunities within Singapore's thriving biomedical innovation ecosystem. Join us in shaping the future of RNA-based medicines and establishing Singapore as a world-class hub for nucleic acid therapeutics.

The above eligibility criteria are not exhaustive. A*STAR may include additional selection criteria based on its prevailing recruitment policies. These policies may be amended from time to time without notice. We regret that only shortlisted candidates will be notified.

This role is with NEU Battery Materials , a startup supported by SGInnovate.

Overview

NEU Battery Materials aims to be the largest, cleanest, and most neutral source of recycled lithium globally. The firm developed the world’s first patented electrochemical redox recycling method that only uses electricity and water. This revolutionary approach is paving the way for a more sustainable future in LFP battery recycling.

We are expanding our current scale of operations and are seeking an experienced Head of Research & Development . This new teammate will play a crucial role in the battery recycling process through development and scale-up to commercialization. Working closely with the Engineering team, this hire will lead, drive, and execute the R&D roadmap in collaboration with the CTO to develop cutting-edge recycling equipment for the advancement of pilots and concepts to scalable, refined commercial products.

Responsibilities

Scientific & Technical Leadership

• Set direction and roadmap for the research team, aligning with the company goals and milestones
• Work closely with the CTO to manage and shape NEU’s technical strategy
• Demonstrated ability to lead and grow high-performing technical teams through clear goal-setting, structured mentorship, and a culture of accountability and trust
• Track team progress, troubleshoot challenges and roadblocks, and provide scientific guidance
• Drive IP development and maintenance while managing the filing of patents, grant applications, and technical due diligence processes to protect intellectual property
• Design, implement, and oversee experiments aimed at enhancing lithium recovery efficiency, purity, and cost-effectiveness in the recycling of LFP batteries
• Supervise data analysis, documentation, and reporting to ensure high-quality insights for both internal teams and external stakeholders, including investors, customers, and regulatory bodies
• Uphold scientific integrity and reproducibility across all R&D activities, ensuring alignment with NEU Battery Materials' commitment to innovation and sustainability

Process Optimization & Scale-Up Support

• Collaborate closely with process engineering team to pilot novel recycling technologies and facilitate the scale-up of laboratory breakthroughs for industrial applications
• Identify and troubleshoot technical bottlenecks in the redox recovery process and propose solutions to optimize material recovery and improve process efficiency
• Act as a critical bridge between bench research and the pilot line, ensuring seamless translation of R&D innovations into scalable, commercial-ready processes

Requirements

• PhD or MS in Electrochemistry, Materials Science, Chemical Engineering, or a related discipline
• 5–15 years of hands-on R&D experience in battery technology, recycling processes, or industrial electrochemistry
• Strong foundation in electrochemical principles, including thermodynamics, kinetics, mass transport, electrodeposition, and catalyst preparation techniques.
• Proven experience in scaling up lab-scale technologies to pilot or production-level systems
• Strong track record of building, managing, and mentoring high-performing research teams
• Excellent project management and communication skills, with the ability to engage cross-functional stakeholders and external partners
• Entrepreneurial mindset with a proactive approach to experimentation, innovation, and problem-solving in a fast-paced startup environment

Interested candidates may apply directly at:

• Seniority level Director

• Employment type Full-time

• Job function Research, Science, and Strategy/Planning
• Industries Chemical Manufacturing, Research Services, and Chemical Raw Materials Manufacturing

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