210 Pharmaceutical Development jobs in Singapore

Product Specialist Role

As a Product Specialist, you will play a pivotal role in promoting pharmaceutical products to Medical Practitioners and Allied Health Professionals in clinics and hospitals. You must possess in-depth knowledge of the relevant therapeutic areas concerning the products, specifically anti-infectives and psychiatry.

• Maintain up-to-date expertise on company products, branding strategy, positioning, customers, and competitors in the relevant therapeutic areas.
• Drive territorial management through sales reports analysis and market intelligence gathering.
• Deliver accurate weekly sales forecasts to achieve top-line sales targets.

Working closely with existing customers is essential to build strong relationships and proactively seek new accounts to secure in Singapore. Engaging with Key Opinion Leaders (KOLs) is crucial for expanding your network.

Job Description
Identify and capitalize on new market opportunities to expand the customer base, increase market penetration, and drive year-on-year revenue growth.
Proactively prospect, network, and generate leads within the Healthcare, Pharmaceutical, or biosafety lab user sectors.
Build and maintain strong relationships with key clients and partners to drive repeat business and customer referrals.
Monitor competitors and industry trends to remain agile and benchmark offerings effectively.
Collaborate closely with the CEO, Finance, and Operations teams to align initiatives and ensure seamless execution.
Track and report key performance metrics, including sales volume, forecast accuracy, market share, and revenue growth.
Provide regular updates and actionable insights to senior management to support data-driven decision-making.
Requirements:
Degree in Business, Marketing, or Engineering from a reputable university.
Minimum 8-10 years of experience in sales.
Proven track record of consistently meeting or exceeding revenue and profitability targets.
Background in industries such as FMCG, logistics, B2B services, pharmaceuticals, or public sector (e.g., Ministry of Health) is preferred.
Strong leadership, communication, and negotiation abilities.
Proficiency in sales analytics, CRM platforms, reporting tools, and forecasting methodologies.
Excellent problem-solving and decision-making capabilities.
Demonstrates integrity, professionalism, and thrives in a dynamic, fast-paced environment.
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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.
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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 using Quality by Design (QbD) principles, supporting production from early-stage research through preclinical and pilot-scale batches. The successful candidate will also drive technology 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.
• Apply QbD principles to 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.
• Lead tech transfer activities to 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 of tech 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.

Company description:

SingHealth Polyclinics, a leader in family medicine, provides seamless, patient-centred and preventive healthcare that is affordable and accessible to all. SingHealth Polyclinics' network of polyclinics provides primary healthcare services to the community. It plays an integral role in promoting a healthy lifestyle within the community and empowering families with the knowledge of common health issues, care and treatment options. SingHealth Polyclinics is a member of Singapore Health Services (SingHealth) - a public healthcare cluster which also manages three hospitals and five specialty centres.

Job description:

Job Description

You will assist Principal investigators in conducting clinical trials & research projects according to Singapore Good Clinical Practice (GCP) guidelines. You will plan, organise & coordinate workflow of study projects from initiation to completion phase, perform screening and recruitment activities as well as compile relevant patients' data and maintain proper study documentation according to established protocols and regulatory requirements. Additionally, you will facilitate coordination of research studies with funding and regulatory bodies. Other duties include providing administrative support for Research Department when the need arises.

Requirements:

• Life Science or Nursing Degree holder. Candidates with Nursing Diploma must have minimum 2 years of relevant experience
• At least 1-2 years of experience in clinical research coordination
• Ability to converse in mainstream languages (able to speak in local dialects will be an added advantage) to handle patient queries on the research study
• Strong organizational skills, able to work independently and/or a team player, meticulous in details
• Proficient with MS Office applications

You will be part of the research team involved in various clinical projects and will be required to perform the following:

• Act as a liaison between study participants and the research team; provide study participants with clear explanation of purpose of study and assist with obtaining informed consent

• Schedule participants for visits to clinic for the required tests and evaluations, collect their samples and assist in monitoring the participants' well-being

• Assist with compilation and management of patient data; ensure study is conducted in compliance with study protocols, established procedures and timeline

• Draft reports for submission to the relevant authorities

• Tabulate and document financial payments received or made to the study

Job Requirements:

• Bachelor's Degree in Nursing/ Medical Technology / Health Science / Life Science / Pharmacy
• Proficient in Microsoft Office Applications

The Laboratory of Surgical System & Service Innovation (3SI) is a multi-disciplinary laboratory that provides a platform for cutting-edge surgical health services research that informs healthcare systems, policies, and programs to provide high-value, patient centered care for patients and their families undergoing surgery.

We are looking for an enthusiastic, dynamic, meticulous, and responsible Research Coordinator to work closely with a team of experienced researchers and the clinical team in health system, services innovation, and novel surgical technologies research. You will be part of a holistic clinical and health services research team whose mission is to improve clinical outcomes for seriously ill patients undergoing major surgery.

Responsibilities:

• Patient recruitment & consent
• Data Collection, Management, Analysis
• Research Grant support
• Prepare and submit IRB applications, amendments, continuing reviews, and study closures
• Administrative Support (eg. Process claims, reimbursements, and invoices for team members)
• 1 year experience in research administration, IRB-related work and patient consenting required
• Any ad hoc duties required

Job requirements:

• Bachelor's degree in a relevant field (e.g., life sciences, public health, research administration, nursing, ethics)
• Fresh grads are welcome to apply
• Interest in scientific research and willing to engage in various aspects of the research processes
• Proficient computer knowledge (MS Office – Word, Excel, PowerPoint)
• Good interpersonal skills

Salary: up to $4000

Duration: 6 months contract

Working Days & Hours: Mon-Fri Office Hours

Location: Jurong

Job Description:

Subject Recruitment and follow up

• Be involved in subject recruitment, scheduling and data entry. Screen patients based on study eligibility, and communicate the study aims to potential subjects in layman terms.
• Obtain consent taking, administer study questionnaires and follow-up on study participants.
• Work closely with research team, clinicians, clinic staff and other relevant internal departments to ensure research study needs are met.
• Able to work on tight timelines, set sensible targets and achieve research deliverables.

Research Documentation / Administrative duties

• Conduct research study activities like patient recruitment, data collection and data management.
• Assist in data collection from electronic health records.
• Set up and maintain study investigator files, including records of consent taken and blood collection.
• Maintain study records in databases such as Redcap and in electronic health record systems.
• Responsible for maintaining strict adherence to research protocols i.e., HBRA.
• Liaise with investigators, clinicians and laboratory team to set up clinical workflows at multiple clinical departments for research recruitment.
• Prepare necessary documentation for audit purposes.
• Coordinate the submission of new IRB applications, study amendments and annual reports.
• Maintain the highest standard of professional conduct and record keeping in accordance with hospital policies, ethics requirements and local regulations.
• Assist with any other duties of a similar nature that are delegated by the PI.

Job Requirements: Min Degree in Life Sciences or similar

Interested candidates, please submit your resume to:

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R

The SINGAPORE EYE RESEARCH INSTITUTE (SERI) serves as Singapore's national research institute for ophthalmic and vision research. SERI functions as the research arm of the various clinical ophthalmic centres in Singapore including the Singapore National Eye Centre, the National University Health Systems (NUHS), Tan Tock Seng Hospital etc., and further works in collaboration with Duke-NUS Graduate Medical School and various biomedical research institutions, as well as major eye centers and research institutes throughout the world. SERI has developed a world-leading reputation in broad-based clinical translational research and epidemiological programmes for many eye diseases, particularly disease relevant to Asia. SERI currently has close to 200 staff with an annual budget of $20M.

Clinical A/Prof Anna CS Tan is a Principal Investigator working in medical retina conducting study that is focused on studying patient-centered outcomes and methods to improve patient's adherence to long term treatment for chronic retinal diseases. She is inviting passionate, committed candidates interested in improving patient care for the position of Clinical Research Coordinator (CRC).

Position Summary

As a CRC, you will execute best practice clinical research to support quantitative and qualitative data collection to help assess patient reported outcomes and implement interventions aimed at improving adherence to treatment and follow up for chronic eye diseases. You will be involved in the planning, development, and oversight of the day-to-day clinical activities for specified clinical research initiatives, as established by the principal investigator (PI) You will be expected to provide support for an array of duties related to the various study protocol, including recruitment of English and Mandarin-speaking study subjects, case notes extraction, questionnaire administration, and managing the study sample database. You will also develop and administer budgets and operating procedures for the project, coordinating day-to-day administration related interactions with associated departments, agencies, and vendors. Flexibility to work on multiple projects sharing similar protocols, a natural aptitude for organization, and being deadline-driven are important attributes for this dynamic position.

Job Description

• Plan, schedule and carry out day-to-day study procedures such as recruitment of participants and collection of high quality clinical and patient-related data
• Following training and validation, conduct refraction, administer questionnaires, and carry out other clinical procedures as specified within the relevant study protocols
• Prepare various study materials (invitation letters, brochures, screening log forms, etc.).
• Ensure that all clinical activities are carried out in accordance with established research protocols and in compliance with applicable laws, regulations, policies, and procedural requirements
• Undertake data entry and preparation of reports to share the study status (e.g., recruitment etc.,) with the supervisor
• Serve as the primary point of liaison between investigators, ancillary departments, regulatory bodies, and research participants
• Perform other job-related duties, as assigned

Requirements

• Diploma/degree in Optometry, Social Sciences, Psychology, or other health or science-related disciplines
• Strong communication (especially spoken and listening) and interpersonal skills, leadership, and people management skills
• Excellent organizational and analytical skills with project management experience
• Experience administering survey questionnaires and collecting clinical data from study participants
• Computer competency including proficiency in MS Office (Word, Excel, PowerPoint)
• Ability to manage multiple projects simultaneously and effectively work in teams
• Have a pleasant and engaging demeanour
• Able to work from Mondays to Fridays and on alternate Saturdays. Might be required to work after-office hours (only when required for certain occasions).
• Candidates without experience are welcome to apply

Preferred

• Experience working with a wide variety of stakeholders (patients, doctors, nurses, researchers, admin staff etc.) and ability to manage group dynamics effectively