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.