Mô tả công việc
Company Description Danapha Pharmaceutical JSC is a leading Vietnamese pharmaceutical company with over 60 years of experience in developing and manufacturing high-quality medicines. The company operates three manufacturing plants in which one is compliant with EU-GMP and a dedicated R&D center.
Role Description This full-time on-site RD Analyst role is based at Danapha Pharmaceuticals in Đà Nẵng. The RD Analyst will support research and development activities by designing and executing laboratory experiments, analyzing data, and contributing to the development and optimization of pharmaceutical formulations and processes. Daily responsibilities include preparing and testing samples, documenting methods and results in accordance with regulatory and internal quality standards, and collaborating closely with scientists, production teams, and quality assurance. The role also involves participating in method validation, preparing technical reports, assisting with regulatory submissions, and helping implement new technologies or processes in line with EU-GMP and other relevant guidelines.
Qualifications
- Strong analytical and laboratory skills, including experience with experimental design, data collection, and interpretation.
- Knowledge of pharmaceutical R&D processes, formulation development, and method validation in compliance with EU-GMP or equivalent standards.
- Familiarity with quality systems, documentation practices, and regulatory requirements relevant to pharmaceutical products.
- Proficiency with common scientific and data analysis software; ability to prepare clear technical reports and presentations.
- Bachelor’s degree or higher in Pharmacy, Pharmaceutical Science, Chemistry, Biochemistry, or a related field.
- Strong attention to detail, problem-solving abilities, and capacity to work accurately under time constraints.
- Effective communication and teamwork skills, with the ability to collaborate across R&D, production, and quality functions.
- Prior experience in a pharmaceutical R&D or QC/QA laboratory is an advantage; understanding of international markets is a plus.