上海招聘

职位描述：
1. Job Purpose (Why does job exist?)

1.1 该职位支持生产进行炼胶及压模生产过程中的质量检验及最终产品的检验，以符合顾客的质量要求。
 This position supports the production to perform quality inspection in the compounding process, molding process and the finished goods to meet the quality required by the customer.

1.2 主要目的是传递产品的成本效应，但不会危害到产品的标准性能，可靠性和质量。
    Our main goal is to deliver products that are cost effective, but without jeopardizing the required standard of performance, reliability and quality.

1.3 所有员工须根据公司的质量政策来约束自己的行为。
All employees should at all times perform their activities in accordance with the quality policy of the company.


2. Job Responsibilities/Objectives

2.1 微生物实验室所有日常的来料，过程样及成品的检验测试。
Test all routine incoming, in-process and final release of materials and products in micro lab.

2.2 微生物实验室所有由生产，工艺及客户申请的非日常测试分析。
All non-routine analyses requested by production, process departments and customers in micro lab.

2.3 负责洁净区的监测，协助水系统的监测分析，压缩空气的监测。
In charge of the monitoring of cleanrooms and support of the monitoring of water system.

2.4 维护及提高微生物实验室的质量体系----包括OOS，偏差，偏离，变更，文件及其它。
        Maintain and improve quality systems in the micro laboratory---OOS, deviations, excursions, change controls, documentation and others.

2.5 对微生物实验室的设备，设备仪表，耗材库存进行维护管理，来保证足够安全的量来进行日常测试及分析。
       Be responsible for maintaining the micro laboratory facilities, instrumentations, micro inventory for proper functioning of the laboratory, while maintaining quality budge and safety expectations.

2.6 定期地检查微生物实验室测量仪器和使用的设备。
       To handle the inspection gauges and equipment used appropriately in micro lab.

2.7 实验室仪器的验证，日常维护及校准工作。
       Lab equipment validation, maintenance and calibration.

2.8 将任何在控制下的偏差问题及质量问题反馈给管理者和工程师。
       Feedback to Supervisor /Engineer any problems on deviations and quality issues which are beyond
       your control.

2.9 完成质量经理及实验室组长布置的其他工作。
 Conduct any other job assigned by QA head and direct supervisor.

2.10 始终遵守GMP。
       To comply the cGMP always.


3. Job Requirements

3.1 良好的沟通能力与团队合作精神
       Good communication skill , with team work spirit.

3.2 良好的计算机能力
Good computer skill.

3.3 良好的英语（读，写）
Good written and reading English skill.


4. Skills, Knowledge & Experience – Professional, Technical

4.1 生物，制药或者其他相关专业背景
       With education background majored in biological, pharmaceutics or relevant education background.

4.2 1年以上质量部门QC工作经验
With at least 1 years of working experience in Quality department as QC. 举报 分享

About West
West Pharmaceutical Services, Inc. is a leading manufacturer of packaging components and delivery systems for injectable drugs and healthcare products. Working by the side of its customers from concept to patient, West creates products that promote the efficiency, reliability and safety of the world's pharmaceutical drug supply. West is a listed company in NYSE and named to the S&P 500 Index in 2020.
Headquartered in Exton, Pennsylvania, it supports its customers from locations in North and South America, Europe, Asia and Australia. West's 2019 net sales of $1.84 billion reflect the daily use of approximately 100 million of its components and devices, which are designed to improve the delivery of healthcare to patients around the world.
西氏医药包装是全球领先的注射剂容器包装和给药系统生产厂商。从概念设计到患者，西氏携手客户，制造的产品可以提高全球药品供应的效率、可靠性和安全性。西氏是纽交所上市公司，并于2020年被纳入标准普尔500指数。总部位于宾夕法尼亚州埃克斯顿（Exton, PA），西氏在北美、南美、欧洲、亚洲和澳大利亚等地设有分部为客户提供支持。 西氏2019年的净销售额为18.4亿美元，日生产组件超过1亿个，旨在为全球病患带来更好的医疗保健服务。

About West Asia Pacific
In 1983, West established operations in Singapore in the Asia Pacific region. In 2009, an injection molding facility opened in Shanghai Qingpu Industrial Zone in China. At present, West has two digital technology centers in Bengaluru India and Taiwan China, three main production bases located in Singapore, Shanghai China and Chennai India, and seven offices and distributor centers in Australia, China, India, Korea, and Singapore.
1983年，西氏率先在亚太区的新加坡设立工厂；2009年，在上海青浦工业区开设了***家注射成型工厂。目前，西氏分别在印度班加罗尔和中国台湾拥有两个数字技术中心，在新加坡、中国上海和印度钦奈设有三个主要生产基地，并在澳大利亚、中国、印度、韩国和新加坡设有七个办事处和分销中心。