Responsibilities:
61Manage a group of analysts and project activities.
61Provide high quality, on-time testing in compliance with regulatory requirements to support on-going QC projects.
61Write and review GMP and technical documents, such as SOP, analytical method, method qualification/validation protocols/reports etc.,
61Communicate with internal/external partners or clients to ensure timely completion of assigned word.
61Support management team to carry out departmental objectives.

Requirements:
61Master or bachelor degree with major in Chemistry, Biochemistry, Molecular Biology, Biological Engineering or related field, minimum 3 years of relevant industry experience for master, minimum 5 years of relevant experiences for bachelor degree.
61Knowledge and expertise in some the following fields: Chromatographic and spectral techniques related to HPLC, UPLC, GC, CE, icIEF etc.;
61In-depth knowledge in FDA/EMA/CFDA cGMP regulations, Pharmacopoeias, and ICH guidelines.
61Good communication skills in English and Chinese, fluent in writing and reading in both languages.
61Critical thinking, scientific reasoning and problem-solving skills.