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SHDM IVD Quality Control Bioch

刷新時(shí)間:2023-11-27

西門(mén)子醫(yī)療系統(tǒng)

面議

上海市 | 本科 | 1-3年

基本信息
工作地點(diǎn):上海市 所屬部門(mén):SHDM 西門(mén)子實(shí)驗(yàn)系統(tǒng)(上海
職位類(lèi)別:質(zhì)量檢驗(yàn)/測(cè)試 招聘人數(shù):1 人
匯報(bào)對(duì)象:無(wú)
職位描述

We at Siemens Healthineers? are committed to helping healthcare providers globally to succeed in today’s dynamic environment. We are inspired to transform the way things are done – because we want what is best for our people, our customers and ultimately the health of mankind. While we are invested in engineering excellence – leading-edge medical technologies and services, we don’t stop there. We’re also deeply invested in our 46.000 people with the hearts of pioneers and minds of engineers, highly committed and connected in this industry. And as we strive to shape the future of healthcare, our overall success will depend on our ability to continuously reinvent ourselves.

If you are ambitious and change makes you thrive, help transform Siemens Healthineers into a learning organization.

This Biochemist II position will be responsible for applying scientific principles to accomplish a wide variety of technical assignments for the Immunoassay (IA) Quality Control (QC) group for the new manufacturing facility in Shanghai.
?Accurately assess testing data to ensure product specifications are met and DHR is compiled in a compliant manner, according to current cGMP and site SOP’s (routine record witnessing)
oAssess daily, the current staffing levels in conjunction with product due dates and perform data witnessing, initial uation, or troubleshooting guidance with a focus on production opportunities
?Initiate and support discussions and s with internal and external key work groups in support of processes to release product (execute timely and appropriate involvement of Technical Operations (TO), support production flow)
oAttend meetings with TO as needed to support less experienced Biochemist, or in the absence of the product Subject Matter Experts
?Create an initial path forward for addressing OOS, and non-compliant DHRs (initiate re-uation forms, retests, initial assessment)
oUse tracking sheets and batch records to assess products lifecycle within the QC department, looking for efficiency gains and missed opportunities
?Problem solving – has a working knowledge of available tools related to job function and incorporates the different databases, applications, personal knowledge, and individual experiences when necessary
oMaintain understanding of current tools, and adopt and champion new tools
?Initiate and drive complex and impactful process, and/or environment, and/or employee improvements (observe, identify, and communicate ideas to improve the day to day responsibilities and job satisf of the entire team)
oConstruct at least one high level initiative which has team or departmental impact.
?Help to reach department goals and ives through collaboration and influence (utilize teamwork/ collaboration with other department members be influential in order to help the department reach their goals)
oAttend and support new assay and platform harmonization meetings and activities as needed
?Function as a leader within QC be able to represent and support the interest of QC, internally and externally of the department work with all QC supervisors to identify mutual challenges and solutions
?Ability to travel domestically and internationally

This position may suit you best, if building learning organizations is your expertise and you have extensive experience with Top Management Learning and Leadership Development.

?EDUCATION:
oBachelor’s Degree (or equivalent degree) with a discipline in Biology, Chemistry, Biochemistry, Biotechnology, Microbiology, Molecular Biology or Medical Technology is required.

?EXPERIENCE:
o3-6 years’ experience working in a similar role in the medical diagnostic/medical device, FDA-regulated laboratory industry.
oPrior experience manufacturing commercialized automated immunoassays and/or ELISA and chemiluminescent products is preferred.

?REQUIRED SKILLS:
oExcellent verbal/written communication skills and organization/time management skills
oHigh attention to detail and commitment to accuracy
oVerbal/written proficiency in English.
oProficiency with Microsoft Office applications
oAbility to work individually and in team settings

崗位要求:
學(xué)歷要求:本科 工作經(jīng)驗(yàn):1-3年
年齡要求:不限 性別要求:不限
語(yǔ)言要求:普通話 專(zhuān)業(yè)要求:不限
企業(yè)信息
公司性質(zhì):其它 公司規(guī)模:10000人以上
所屬行業(yè):醫(yī)療設(shè)備/器械
企業(yè)信息

西門(mén)子醫(yī)療系統(tǒng)

醫(yī)療設(shè)備/器械

10000人以上

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