Job Responsibilities 工作職責(zé)
1、Responsible for the related work of visual inspection and packaging.
負責(zé)燈檢和包裝的相關(guān)工作;
2、Ensure operations strictly adhere to all QA-Controlled documents (such as SOPs, Batch Records) and cGMP/Quality requirements;
確保操作嚴(yán)格遵守所有QA控制文件(例如SOP、批記錄)和cGMP/質(zhì)量要求;
3、Responsible for the cleaning and disinfection of rooms and equipment in the responsible area;
負責(zé)責(zé)任區(qū)域的房間和設(shè)備清潔和消毒;
4、Generate and review documents for related manufacturing processes;
起草和審核相關(guān)步驟生產(chǎn)流程文件;
5、Responsible for the submission requirements of the production materials for the post.
負責(zé)本崗生產(chǎn)用物料的提交需求;
6、Responsible for completing various trainings organized by the workshop and the company on time.
負責(zé)按時完成車間及公司組織的各項培訓(xùn);
7、Complete other tasks assigned by supervisors.
完成上級領(lǐng)導(dǎo)安排的其他任務(wù)。
Qualification 任職資格
1、Bachelor's Degree in Chemistry, Chemical Engineering, Life Sciences or relevant background.
本科學(xué)歷,專業(yè)是化學(xué),化學(xué)工程,生命科學(xué)等同等專業(yè)。
2、2 years or above experience in visual inspection and packaging of injection.
2年或以上的注射劑目檢和包裝工作經(jīng)驗;
3、Be familiar with the pharmaceutical industry, and willing to engage to biopharmaceutical industry, good learning ability and good team spirit.
對制藥行業(yè)有一定認識,并且愿意從事生物醫(yī)藥行業(yè),學(xué)習(xí)能力強和好的團隊意識;
4、Capable of writing detailed reports and summaries and exhibit detail oriented documentation skills. Communicate effectively and work professionally in a team environment.
能夠撰寫和總結(jié)工作報告。在團隊中高效的溝通和專業(yè)地工作;
5、Familiarity of computer-based systems.
熟悉計算機操作。
6、Oral and written communication skills in English and Mandarin (Read, Write, Verbal).
有良好的英語和普通話口語和寫作技能(閱讀,寫作,口語)。