长沙招聘

Position Purpose / 职位描述

Guided by J&J, XJP new product development guidelines, global APLA PDMS organization guidelines and aligned with company strategic objectives under the leadership of PDMS Xian Manager, the holder of this position shall implement new analytical methods transfer or verification or validation or development of related products, carry out related analytical tests for establishing methods purpose to ensure timely & correct methods of specified projects, and implement a part of sample testing to coach QC analysts and ensure quality of new methods.


Responsibility / 职责

1. For new product: Method Development / Method Validation /Method Transfer, review and understand the transfer files. Includes product and ingredients. The analytical methods can be executed correctly. The developed methods fit to QC lab. Responsible to establish the specifications and methods after development / validation / transfer; Carry out analytical validation after development. Update related specifications and methods for new product before the product launch.
2. For marketed product: new methods improvement / development / validation, for the purpose of analytical compliance gaps and new technology development, establish methods.
3. Test related samples for the purpose of training QC analysts or establishing methods.
4. Net works and collaborate with related functions according to project timeline and make sure to finish projects on time.
5. Compliance. Draft specifications and methods complied with XJP and PDMS policy.
6. Know all position-related requirements for environmental, safety and industry hygiene, and comply with all these requirements.
7. Documentation. Draft and revise related protocol and report for analytical 1, 2 items, whatever project assigned by Xian-Janssen or PDMS.

Requirements & Qualifications / 职位需求

1. Bachelor or above degree on pharmacy, chemistry, biochemistry and other related majors.
2. Over 2 years working experience in pharmaceutical analysis.
3. Fluent English in writing and speaking.
4. Good knowledge on pharmaceutical analysis, trends of local & international regulatory & statutory environment & quality processes.
5. Have analytical development ability and have experiences on this area, manipulation skill to analytical instrument.
6. Good interpersonal, communication and presentation skills

公司简介(中文) 恢复为 “成立于1985年的西安杨森制药有限公司（“西安杨森”）是中国***的合资制药企业之一，也是中国改革开放以来进入中国的最早一批制药公司之一，其总部位于北京的中央商业区。西安杨森是强生公司的一员。从创立之初，西安杨森就致力于引进和生产许多创新产品和高质量产品。西安杨森一直致力于投资未来，计划增加在生物制品、心脏病学、风湿病学和泌尿科学领域的新系列产品。西安杨森致力于利用这些新药改善中国患者的医疗保健状况。

本着公司信条和关爱精神，西安杨森一直是活跃的企业公民，在医药、公共卫生、药物研发领域和企业社会责任方面从事了五十多项合作项目。例如，西安杨森与中国卫生部国际卫生交流与合作中心合作创立了“吴阶平医学研究奖和保罗•杨森药学研究奖”，旨在鼓励医药学领域的工作者不断创新。在过去的17年中，共计305名杰出医药学工作者在45个专业领域获得了该奖项，他们在科研领域做出了大量有价值的创新。 此外，西安杨森也被誉为培养制药行业人才的摇篮。1999年，西安杨森被财富杂志（中文版）评选为“中国最受敬仰的十大外资企业之一”。2005年，西安杨森被中国中央电视台评选为“***雇主”，并且分别在2008年、2009年和2010年获得了“中国大学生***雇主奖”。

目前西安杨森所有的招聘信息仅通过前程无忧，智联招聘和猎聘网进行发布，任何在非上述三家招聘网站看到的信息均非西安杨森正式发布。为避免对您的合法权益造成伤害，请务必通过正规渠道投递简历。

2013年，强生在西安高新区投资兴建强生全球供应链先进的生产基地，该项目建设目前已正式启动。新生产基地占地267,000平方米，将取代西安杨森在西安新城区现有的生产基地，成为强生供应链在亚洲的创新枢纽，从而更好地满足中国和其他新兴市场不断增长的需求。新的生产基地将采用世界***的制造技术和先进的质量体系，并引进集电子批号记录和数据存储于一身的全自动化配方生产操作系统以及先进的德国进口生产工艺设备。