職位描述
工作地點(diǎn)：廣東中山市
工作性質(zhì)：全職
性別要求：不限語(yǔ)言：精通的英語(yǔ)，精通的其他
崗位職責(zé):
1 Performing analysis test of FP, ST and FUST according to Novartis Control procedure and local registration analytical methods strictly, supply accurate results in time.
2 Carry out analysis for process validation of product.
3 Conduct special analysis investigation, method development and validation.
4 Conduct those urgent tests and work to be required by supervisor.
Special Tasks
1 Revise related GLP/SOP according to Novartis Quality Policy as well as local regulatory requirements as arranged by supervisor.
Others
1. Ensure all activities in line with cGMP.
2. Observe BNP SOPs and be punctual according to working time schedule.
3. Keep assigned working place clean and tidy all the time.
4. Economize on water, electricity, solvent and others in work.
5. Strong team spirit and positive toward working attitude.
6. Attend to any other work related assignment, which may be given by supervisor.
任職條件:
制藥及相關(guān)專業(yè)，大專以上學(xué)歷；
5年以上QC理化分析經(jīng)驗(yàn)；經(jīng)驗(yàn)稍弱者可應(yīng)聘質(zhì)檢技術(shù)員。
熟悉各種分析儀器；
熟悉GMP相關(guān)知識(shí)；
溝通良好。
其它福利:
班車(chē)及午餐
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