266 Pharmaceutical Development jobs in Singapore

We are seeking a results-driven individual who excels in a fast-paced sales environment. This full-time position offers an exciting opportunity to leverage your expertise in the healthcare and medical industry to build strong relationships with healthcare professionals and drive sales of our pharmaceutical products.

Job descriptions

• Identify and cultivate new sales opportunities.
• To service & maintain relationships with key accounts in hospitals/medical centres/GPs/Pharmacies.
• Provide exceptional customer service and support to existing clients, building long-term, trusted relationships.
• Coordinate and implement sales/marketing action plans(e.g. plan sales routes, make regular calls/visits, sales presentation, sampling, etc.).
• Maintain detailed records of sales activities and customer interactions.
• Achieve and exceed sales targets through effective territory management and strategic account planning.

Requirements

• Diploma/ Bachelor's Degree or equivalent.
• Strong communication and interpersonal skills, with the ability to build rapport and influence key decision-makers.
• Demonstrated ability to work independently and as part of a team to achieve sales goals.
• Effective time management and organisational skills, with the ability to prioritise tasks and meet deadlines.
• Sales experience in the pharmaceutical industry is an added advantage.
• Fluency in English, both written and spoken. Additional languages are an added advantage.
• Possess own transport (preferably).
• Singaporeans, Permanent Residents or EP holders.

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.

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Job Category: Research

Posting Date: 27 Mar 2025

Job Description:

You will provide research support service for clinical research, in accordance to the applicable regulatory, Good Clinical Practice and protocol requirements. You will work closely with the Principal Investigators (PIs), to assist them with organisation of study initiation meetings, IRB submission, protocol development, preparation of study logistics, recruitment, data collection and management, study documentation, study monitoring and other duties as assigned.

You will support and participate in the SGH mission of providing quality patient care, education, and research.

Job Requirements:

1. Bachelor Degree in Nursing/Science or Diploma in Clinical Trials Management
2. Fresh graduate or with at least one year of relevant experience
3. Proficient in using MS Office software
4. Effectively bilingual
5. Excellent oral and written communication skills

National Cancer Centre of Singapore Pte Ltd

Job 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

National Neuroscience Institute of Singapore

Job 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:

1. Contribute to clinical trials set-up, feasibility and coordination
2. Contribute to data processing and analysis of results for multiple studies conducted within the department
3. Acquire new skillsets, such as imaging handling, processing and analysis
4. Gain experience in scientific writing for presentations and publications

Requirements:

1. Bachelor’s degree in Life Sciences, Psychology or related fields
2. Good communications and interpersonal skills
3. Good IT literacy and statistics skills are also desirable
4. Prior experience in a clinical environment and/or with clinical trials/studies would be most advantageous

Job Responsibilities:

• Manage and execute clinical projects and related administrative tasks in a fast-paced environment.
• Ensure proper documentation and maintain an up-to-date database.
• Perform regular maintenance and calibration of clinical equipment.
• Handle data entry and collect accurate clinical data.
• Plan and schedule subject visits, including coordinating recruitment activities.

Job Requirements:

• Possess at least a Diploma or Degree in a relevant field.
• Able to work independently and meet tight project deadlines.
• Strong team player who can also work with minimal supervision.
• Capable of prioritizing tasks and managing multiple responsibilities efficiently.
• Excellent coordination, communication, and interpersonal skills.
• Able to thrive in a fast-paced environment and handle work-related stress effectively.

To apply for this position, please email your detailed resume, including your current and expected salary, to .

We regret to inform that only shortlisted candidates will be notified.

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• Assist the investigators in overall administration of clinical research activities prior to, during, and post-study, such as enrolling suitable subjects, taking vital signs, collecting and processing biological samples, collecting and entering data, and monitoring subjects’ condition.
• Work with the study team to ensure subjects’ safety.
• Carry out the required procedures according to the SOP, study protocol, and Instruction manual(s) in compliance with the Regulations and ICH Good Clinical Practice Guideline.
• Attend investigator’s meetings (local/overseas) and site initiation meetings as assigned, and liaise with relevant internal and external agencies during the course of work.

• Degree in Sciences/Nursing. Those with a Diploma will be considered as Associate.
• Registration with the Nursing Board, Singapore (applicable to State Registered Nurse only).
• At least 2 years’ experience in the coordination of clinical research activities.
• Good team player.
• Problem-solving skills.

Only shortlisted candidates will be notified.

National Neuroscience Institute of Singapore

Clinical Research Coordinator

Job 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