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ONE STOP ENGINEERING PTE. LTD. is seeking a validation professional in Singapore to develop and execute validation protocols (IQ/OQ/PQ, process and cleaning validation) and to author final validation reports. The role involves leading risk assessments and ensuring GMP/GAMP compliance, investigating deviations, and coordinating with QA, Engineering, and...

ONE STOP ENGINEERING PTE. LTD. is seeking a validation professional in Singapore to develop and execute validation protocols (IQ/OQ/PQ, process and cleaning validation) and to author final validation reports. The role involves leading risk assessments and ensuring GMP/GAMP compliance, investigating deviations, and coordinating with QA, Engineering, and...

A leading global pharmaceutical organization is seeking a Director of Quality Risk Management (QRM) to lead and evolve a best-in-class, science-driven risk framework across R&D, Pharmacovigilance, and Medical Affairs. This is a high-impact leadership role with global visibility, shaping how risk-based decision-making is embedded across the enterprise and...

A leading global pharmaceutical organization is seeking a Director of Quality Risk Management (QRM) to lead and evolve a best-in-class, science-driven risk framework across R&D, Pharmacovigilance, and Medical Affairs. This is a high-impact leadership role with global visibility, shaping how risk-based decision-making is embedded across the enterprise and...

Job Description The SingHealth Investigational Medicine Unit (IMU) is a dedicated clinical research unit that supports investigators and sponsors in the conduct of early phase clinical trials and clinical research. Managing clinical trials and clinical research from a diverse therapeutic group such as oncology, infectious diseases, renal and cardiology,...

To assist investigators in conducting clinical trials and research according to study protocol, ICH Good Clinical Practice (ICH GCP), Singapore Human Biomedical Research Act (HBRA) and other applicable regulatory and ethical requirements as well as hospital policies. Job Responsibilities A) Primary Responsibilities and Duties (90%) 1. Compliance with the ICH...

Job Description : Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as an FSP CRA - Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our...

Pfizer in Singapore seeks a QA Operations professional to oversee GMP investigations and related QA systems. You will ensure adherence to PQS and ICH guidelines, maintain inspection readiness, and drive quality improvements with cross-functional teams. The role requires a degree in science and at least 4 years in pharmaceutical QA, with strong communication...

MSD PHARMA (SINGAPORE) PTE. LTD. seeks a Senior Business Analyst to lead automation, analytics and AI initiatives at country level, delivering dashboards and workflows that improve clinical trial efficiency and compliance. You will partner with the CRD and regional teams, translate business needs into specifications, manage end-to-end delivery, and drive...

Novartis Singapore seeks a Clinical Research Associate Manager & Monitoring Services Oversight Manager to lead CRA performance and vendor oversight across clinical trials in Singapore. The role combines people leadership with operational monitoring, ensuring GCP/ICH compliance and optimal CRA resource allocation for sites and studies. Travel may be required;...

Pfizer in Singapore seeks a QA Operations professional to oversee GMP investigations and related QA systems. You will ensure adherence to PQS and ICH guidelines, maintain inspection readiness, and drive quality improvements with cross-functional teams. The role requires a degree in science and at least 4 years in pharmaceutical QA, with strong communication...

RECRUIT EXPRESS PTE LTD is seeking a Clinical Research Associate to conduct pre-study activities, site initiation visits, routine monitoring and close-out visits in line with ICH‑GCP and ClinActis SOPs. You will coordinate with Principal Investigators, assist with site feasibility and investigator/site selection, review CRFs and regulatory documents,...

Singapore National Eye Centre seeks a Senior Lead Clinical Research Associate to oversee clinical research compliance across SingHealth institutions and ensure adherence to regulatory requirements such as HBRA, Health Products Act, and ICH-GCP guidelines. You will plan and conduct monitoring visits, prepare post-visit reports, and recommend preventive and...

Prestige BioPharma in Singapore is seeking a dedicated team member to support and assist product quality related activities. You will help maintain trackers for schedules and completion, manage inventory for retention and stability studies, and assist in preparing, handling, distributing and filing documentation and reports related to quality activities. The...

RECRUIT EXPRESS PTE LTD is seeking a Clinical Research Associate to conduct pre-study activities, site initiation visits, routine monitoring and close-out visits in line with ICH‑GCP and ClinActis SOPs. You will coordinate with Principal Investigators, assist with site feasibility and investigator/site selection, review CRFs and regulatory documents,...

Job description The Singapore Eye Research Institute (SERI) is seeking a detail-oriented Research Compliance and Monitoring Officer to support the oversight and regulatory compliance of clinical trials and human biomedical research studies. This role plays a key part in ensuring studies are conducted in accordance with ICH-GCP, HBRA, HSA regulations,...

Job description The Singapore Eye Research Institute (SERI) is seeking a detail-oriented Research Compliance and Monitoring Officer to support the oversight and regulatory compliance of clinical trials and human biomedical research studies. This role plays a key part in ensuring studies are conducted in accordance with ICH-GCP, HBRA, HSA regulations,...

RECRUIT EXPRESS PTE LTD in Singapore is seeking an experienced Clinical Research Monitor to oversee site activities in accordance with ICH-GCP and SOPs. You will conduct pre-study visits, site initiation, routine monitoring and data verification to ensure study quality. The role involves coordinating with Principal Investigators and sites, negotiating...

Esco Aster Pte Ltd, part of Esco Lifesciences Group, is seeking a QA professional to support GMP readiness and ongoing compliance for cell and gene therapy manufacturing in a cGMP environment. You will oversee deviations, CAPA, change controls, and document reviews on the manufacturing floor in Singapore. The role requires 3-5 years GMP QA experience,...

Recruit Express Pte Ltd. is seeking a 1-year contract Clinical Trial Assistant to support CPMs and study teams with administrative, documentation, TMF, budget management and logistics during clinical trials. You will ensure timely, quality data delivery while complying with SOPs, ICH-GCP, and regulatory requirements. Responsibilities include eTMF setup and...