Job Description

This position will assist in analysis of new 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.
• Expert in working with analytical equipment (HPLC, IR, UV, GC)
• Expert in carrying out Assay, Content uniformity, Impurity tests.
• Ability to work with laboratory instruments such as Dissolution tester, Optical rotation, Friability tester, …
• Carry out chemical and physical control tests on Raw Materials and Finish product according to pharmacopeia’s methods or in-house methods.
• Collect, write, and review technical documents such as CTD & regulatory reports.
• Ability to design document analysis experiments and develop and optimize processes.
• Ability to complete assignments within project-specific timelines.
• Team working in preparing the required documentation for submitting the pharmaceutical dossier into the ministry of health includes CTDs, SOPs, Reports, and ….
• 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

• Master's degree or higher in Chemistry or related educations. • At least 4 years of experience as R&D or QC Expert on pharmaceutical industry. • Age between 27-40 • Gender: female/male • High team work value

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