苏州 [切换城市] 苏州招聘苏州生物/制药/医疗器械招聘苏州医疗器械生产/质量管理招聘

实验室工程师

强生(苏州)医疗器材有限公司

  • 公司性质:外资(欧美)
  • 公司行业:医疗设备/器械

职位信息

  • 发布日期:2017-03-26
  • 工作地点:苏州
  • 招聘人数:1人
  • 工作经验:2年经验
  • 学历要求:本科
  • 语言要求:英语 熟练
  • 职位月薪:5-8千/月
  • 职位类别:医疗器械生产/质量管理  

职位描述

职位描述:
SCOPE OF THE ROLE AND BASIC PURPOSE/职位与基本目的的范围
? The Scientist Level 1/II will report directly to project SAFE quality lead and after training will perform routine testing in compliance with laboratory test methods and procedures to support the manufacturing and timely delivery of product to customers.
? The Scientist 1/II must have the ability to assimilate and apply information rapidly.
? The Scientist I/II will receive general instructions about required tasks and results expected. Work will be well defined and is reviewed for accuracy upon completion.
? The Scientist 1/II is expected to apply standard practices and techniques in specific situations and to recognize discrepancies in results and follow operations through a series of detailed steps and processes. Additionally, the Scientist Level 1 has accountability and ownership to maintain laboratory instruments in their qualified state.
KEY RESPONSIBILITIES/TASKS (indicate estimated % of time spent where possible)/ 主要职责/任务(以时间的百分比表示)
1. 80% - Quality
2. 10% - Operations, engineering, facility, maintenance and purchasing, etc.
3. 10% - Contract Lab

ACCOUNTABILITIES/KEY MEASURES/职责/主要衡量指标
? Performing with competence, upon training, routine testing following laboratory test methods and procedures.
? Developing a competence, upon training, in the use of laboratory instruments and equipment.
? Performing daily calibrations/verifications and routine maintenance of laboratory instrumentation and equipment according to current SOPs.
? Working in compliance with current GMPs with regard to documenting, testing and maintaining accurate laboratory notebooks and data sheets.
? Initiation and participation in laboratory investigations of non-conforming laboratory test results.
? Collecting and preparing laboratory records for evaluation following good documentation practices.
? Responsibility for ensuring personal and company compliance with all national, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.
? Performing other related duties as assigned by management.
Type of Experience/经验类型:
? Lab test experience in Pharmaceutical /medical devices manufacturing sites
Required Competencies and Skills/所需的能力与技能:
? Good interpersonal, organizational and communication skills.
? Self-motivated.
? Familiar with GLP, ISO17025
? Experience on analytical/microbiology testing in MDD or pharmaceutical industry

职能类别: 医疗器械生产/质量管理

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公司介绍

强生(苏州)医疗器材有限公司诚聘

联系方式

  • Email:jjmszl@its.jnj.com
  • 公司地址:地址:span上海