Job Description
This position will assist in the analysis of raw materials and products. The applicant must have a spirit of hard work and patience to achieve the goals. She/he also needs to be motivated to solve technical challenges.
Responsibilities:
- Work with analytical equipment (HPLC, IR, UV, and GC).
- Carry out the assay, content uniformity, and impurity tests.
- Work with laboratory instruments such as dissolution tester, optical rotation, friability tester, etc.
- Carry out chemical and physical control tests on raw materials and finished products according to the pharmacopeia’s methods or in-house methods.
- Collect, write, and review technical documents such as CTD and regulatory reports.
- 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 analysis, such as stability studies.
- Carry out tests on packaging products and materials to evaluate and control the quality.
Requirements:
- Master's degree or a Ph.D. in Chemistry or related fields.
- At least 3 years of experience as a QC expert in the pharmaceutical industry.
- Age range: 27 to 40 years old.
- Gender preference: Male/Female.
- High teamwork spirit.
