Job Responsibilities/工作職責(zé)
1. Perform raw material release testing according to GMP document and SOP;
根據(jù)GMP文件和SOPs的要求檢測原輔料;
2. Perform sampling for raw material, sample retention and send out for contract testing;
對需要檢測的物料進(jìn)行取樣,以及留樣,送檢;
3. Perform instrument maintenance and complete maintenance log;
日常儀器的維護,按照GMP規(guī)程填寫維護日志;
4. Prepare and revised SOPs, review SOP and test data;
編寫和修訂SOPs,復(fù)核相關(guān)的文件以及分析數(shù)據(jù);
5. Other work arranged by superior leaders.
上級領(lǐng)導(dǎo)安排的其他工作。
Job Requirements/崗位要求
1. High diploma’s degree in pharmaceutics, chemistry or biology;
大專及以上學(xué)歷,藥學(xué),化學(xué),生物相關(guān)專業(yè);
2. Has knowledge on analytical instruments, such as IR, NIR, UV, pH meter, HPLC and GC, familiar with GMP regulation;
對分析儀器,如IR,NIR,UV,pH計,HPLC,GC等有一定了解,熟悉GMP法規(guī);
3. Familiar with the drafting of QC operation documents, good at communication;
熟悉QC操作文件的編寫,善于溝通;
4. Excellent oral and written communication skills in Chinese and English (Read, Write, Verbal) demonstrated by communicating with other functions.
良好的中英口語和寫作能力與其他各部門順暢溝通的口語和書面溝通技能。