
QC Reviewer - 生物分析大分子

職位描述
Responsibilities / Duties:
Assists co-workers and internal customers with interpretation of regulatory requirements (e.g., GLPs), SOP requirements, and other guidance documents, as applicable.
Reviews data to ensure quality standards are met and to verify compliance to applicable SOP and regulatory requirements.
Maintains working knowledge of client SOPs and requirements as applicable. Ensures that data reviewed meets applicable client SOPs and requirements.
Performs regularly scheduled audits of departmental systems and supporting data, as applicable, to ensure proper documentation and maintenance (e.g. training files, client SOP reading lists, logbooks, etc.).
Collects error tracking data for items reviewed and reports trends as feedback to the department.
Monitors citation trends in eQA and performs follow-up actions with respondents, management, or others, if needed, to prevent recurring citations, problems, or errors.
Promotes quality and regulatory compliance within the department by working with operations and scientific staff to resolve service/quality issues, serving on a committee, assisting with the development of training programs related to documentation and quality, or other related involvement.
Notifies management of observed quality/compliance issues and service failures.
Participates in quality improvement opportunities and harmonization efforts to promote best practices.
Participates in project debrief meetings as needed.
Facilitates changes to SOPs, policies, training materials, and other documents as applicable.
Completes self-development opportunities.
Performs other related duties as assigned.
Education / Qualifications
Bachelor of Science/Arts (BS/BA) degree.
Ability to efficiently use basic software (e.g., Word, Excel, PowerPoint).
Experience
Two years of laboratory, data review, or related experience with a BS/BA degree.
企業(yè)簡(jiǎn)介
科文斯,全球性的合同研究組織(CRO)Covance Inc.是全球服務(wù)最全面的藥物研發(fā)公司。
我們致力于推動(dòng)醫(yī)療保健事業(yè)發(fā)展并實(shí)現(xiàn)Solutions Made Real?,通過向制藥公司和生物科技公司提供高質(zhì)量的非臨床、臨床前試驗(yàn)、臨床和商業(yè)化服務(wù),幫助減少藥物研發(fā)的時(shí)間和成本。憑借豐富的經(jīng)驗(yàn)與深厚知識(shí),我們具備獨(dú)特的優(yōu)勢(shì),能為客戶合作伙伴提供不僅僅局限于測(cè)試的獨(dú)到見解。
我們還向化學(xué)品、農(nóng)用化學(xué)品和食品行業(yè)提供實(shí)驗(yàn)室測(cè)試服務(wù),同時(shí)也是毒理學(xué)分析服務(wù)、中心實(shí)驗(yàn)室服務(wù)、藥物篩選服務(wù)的市場(chǎng)領(lǐng)導(dǎo)者,以及III期臨床試驗(yàn)管理服務(wù)的全球頂級(jí)提供商。
科文斯官網(wǎng): https://www.covance.com/
職位發(fā)布企業(yè)
科文斯醫(yī)藥研發(fā)(北京)有限公司上海分公司
企業(yè)性質(zhì):外資企業(yè)
企業(yè)規(guī)模:5000-10000人
成立年份:2006
企業(yè)網(wǎng)址:www.covance.com
企業(yè)地址:上海市普陀區(qū)嵐皋路555號(hào)602-606室
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職位發(fā)布日期: 2019-04-25

