● Carry out chemical and physical control tests on raw materials and finish products according to pharmacopeia’s methods or in-house methods.
● Collect, write, and review technical documents such as CTD and regulatory reports.
● Team working on preparing the required documentation for submitting the pharmaceutical dossier to the ministry of health including CTDs, SOPs, reports, etc.
● Conduct development and laboratory analysis such as stability studies.
● Set up analysis methods and carry out the method validation.
● Carry out tests on packaging products and materials in order to evaluate and control the quality.
Requirements
● Expert in working with analytical equipment (HPLC, IR, UV, and GC).
● Expert in carrying out Assay, Content Uniformity, and Impurity Tests.
● Ability to design document analysis experiments and develop and optimize processes.
● Ability to complete assignments within project-specific timelines.
● Ability to work with laboratory instruments such as dissolution tester, optical rotation, friability tester, etc.
● Master's degree or higher in Chemistry or related fields.
● At least 4 years of experience as R&D or QC expert in the pharmaceutical industry.
● Age range: 27 to 37 years old.
● High teamwork spirit.