更新于 2月14日

項目負責人-大分子方法開發(fā)

1.5-2.5萬·13薪
  • 上海浦東新區(qū)
  • 5-10年
  • 本科
  • 全職
  • 招1人

職位描述

藥物分析
    Job Level & compensation offered may vary depending on candidates’ experiences and competencies.
? To perform and supervise the activities of scientific and operational staff responsible for method development/validation projects and analysis of samples.
? Serves as a Study Director / Principal Investigator / Responsible Scientist for research studies. Take on overall responsibility for the technical conduct of a study, analytical direction, review, documentation and reporting of results. All activities are conducted in compliance with appropriate SOPs and regulatory agency guidelines.
? Analyzes biological or chemical samples and/or develops/validates methodologies for various compounds and components in compliance with appropriate standard operating procedures (SOPs) and regulatory agency guidelines.
Responsibilities:
? Documents work and maintains study documentation and laboratory records.
? Independently sets up, maintains, operates and performs routine and non-routine maintenance on general equipment, including problem identification and resolution.
? Informs project management and/or line management of any problems and/or deviations that may affect the integrity of the data and recommends corrective action.
? Promotes a cohesive team environment.
? Suggests and performs modifications to test methods or procedures where precedence exists.
? Provides input and participates in project meetings, plans, monitors and guides project work.
? Serves as lead chemist on projects, overseeing a small group of technical staff, with minimal supervision.
? May interact in external client communications.
? Sets up and performs method development and validation of various analytes in a variety of matrices with limited supervision.
? Organizes, conducts and evaluates analytical results and testing.
? Performs QC review of data.
? Maintains a clean and safe laboratory work environment.
? Performs other related duties as assigned.
? Trains and assists less experienced staff.
? Participates in process improvement initiatives.
? Writes, revises and reviews methods, SOPs and portions of reports and protocols.
? Participates in client visits as needed, assists in communicating technical information.
? Effectively plans and utilizes personnel and resources for timely completion of assigned projects.
? Assists in evaluation of data for incorporation into written reports.

Requirements:
? Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field with min. 5 years of previous laboratory experience. Relevant experience may be substituted for education.
? Ability to perform advanced computer skills (e.g., Word, Excel).
? Experience with use and trouble shooting of analytical equipment is desired.
? Basic knowledge of computers and software programs.
? Familiar with the use of standard laboratory equipment.
? Effective communication (verbal and written), presentation and interpersonal skills.


工作地點

徠博科醫(yī)藥研發(fā)(上海)有限公司3號樓

職位發(fā)布者

許女士/HR

三日內活躍
立即溝通
公司Logo徠博科醫(yī)藥研發(fā)(上海)有限公司
徠博科是一家全球領先的生命科學公司,提供創(chuàng)新性、全方位的實驗室服務,為醫(yī)生、醫(yī)院、制藥公司、研究者和患者提供至關重要的信息,以幫助他們制定明確而有信心的決策。依靠在診斷與醫(yī)藥研發(fā)實驗室的經(jīng)驗與能力,徠博科洞見未來,加速創(chuàng)新,以改善健康與生命。當您需要信息以制定明確而有信心的決策之時,徠博科將是您的信賴之源。徠博科總部位于美國北卡羅來納州的伯靈頓,在全球擁有 60,000多名員工,服務的客戶遍布 100多個國家和地區(qū),在美國FDA2022年批準的新藥中有超過80%有徠博科參與研發(fā)和提供各種服務。公司在美國紐約證券交易所的股票代碼為LH,在 2022年財年公布的收入為148.8億美元。
公司主頁