Job Description
This position will assist in the analysis of new products.
- Carry out chemical and physical control tests on raw materials and finished products according to pharmacopeia’s methods or in-house methods.
- Collect, write, and review technical documents such as CTD and regulatory reports.
- Design document analysis experiments and develop and optimize processes.
- Complete assignments within project-specific timelines.
- Prepare the required documentation for submitting the pharmaceutical dossier to the Ministry of Health including CTDs, SOPs, reports, etc.
- Conduct development and laboratory analyses such as stability studies.
- Set up analysis methods and carry out the method validation.
- Carry out tests on packaging products and materials to evaluate and control the quality.
Requirements:
- Expert in working with analytical equipment (HPLC, IR, UV, GC).
- Expert in carrying out content uniformity, and impurity tests.
- Ability to work with laboratory instruments such as Dissolution Tester, Optical Rotation, Friability Tester, etc.
- Master's degree in Chemistry or related fields.
- At least 5 years of experience in R&D in the pharmaceutical industry.
- Age range: 27 to 40 years old.
- Gender preference: Male/Female.
