Job Description

Job Description:

· You will be responsible to independently develop analytical methods for various dosage forms such as tablets, capsules, solutions and suspensions. The methods include but not limited to Assay, Impurities, Dissolution and residual solvents.

· Support Formulation Development by conducting experiments such as assay, impurity, and dissolution, using liquid chromatography, gas chromatography, US/VIS, FTIR, dissolution tester, pH meter and wet chemistry instrumentation.

· Conduct method validation/verification/transfer independently.

· Author method validation/verification/transfer protocols and reports.

· Record results and generate reports following good documentation practices.

· Train junior scientists.

· Perform any other activities as assigned by management.

Qualifications:

· Ph.D degree or Master degree in Chemistry or related fields

· At least 2 years (Ph.D) or 3 years (Master degree) of method development experiences in the Pharmaceutical industry.

· Solid knowledge in Chemistry

· Mass spectrometry experience is preferred

· Ability to development analytical methods independently

· Strong problem-solving capability

· Deep understanding of Pharmaceutical and cGMP regulation

· Excellent work attitude/ethics

· Good time management skill, flexibility, and multi-tasking abilities

· Ability to follow Good Documentation Practice for notebook recording, protocol design and report writing

· Must be a good team player

· Excellent oral and written communication

· Proficient in Microsoft Office

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