工作简介：
1. GMP合规初级咨询顾问。
Junior consultant for GMP compliance.
2. 在GMP工作环境下工作。
Work in GMP environment.
3. 接受欧美工作思维方式。
Open minded to Western Mind-set and working patterns.
4. 开拓自己在咨询行业的潜力。
Opportunity to explore own potentials in the world of consultancy.
5. 接受相关培训。
Receive a serise of trainings.

工作要求：
1. 理工科毕业生，原料药制药行业为佳，IT相关专业亦可。
Graduated with science degree. Preferable with API/Finished dosag form manufacturing background. IT background is ok.
2. 有1至2年的工作经验为佳。
Preferable with 1 or 2 years of working experience.
3. 关注细节。
Strong attention to details.
4. 必须会说英语，要求可以使用英语进行交流，并熟练书写报告和邮件。
English is a MUST. Good oral and written English, including Pharma terminology.
5. 能够适应差旅。
Flexible for travel.
6. 有能力在同一时间进行多项工作；有上进心。
Multitasking; self-motivation.
7. 有良好的时间管理能力。
Good in Time management

In this full-time role, the Consultant will provide validation services for our clients.
Responsibilities include, but are not limited to, the following:
? Collaboration in project teams
? Various roles in the validation process including the creation and execution of qualification protocols (IQ, OQ, PQ)
? Development of validation plans
? Performance of risk assessments.
? In addition, this role requires close interaction with clients and the ability to work and communicate with both team members and external stakeholders.
Requirements:
? Native Mandarin
? Fluent English
? Technical Degree (Engineering, Chemistry, Informatics, Physics, Mathematics)
? Full availability to Travel

Nice to have:
? Fluent in other languages
? Fluent in other languages
? Experience in Pharmaceutical Sector
? Integrity, strong analytical skills and attention to detail

Work Location: Shanghai

上班地址：申滨南路1058号虹桥龙湖天街

PQE公司成立于1998年，作为欧洲领头的整体质量打包解决方案服务公司，以200多名专家咨询师的优势，服务领域包括质量系统、合规注册和验证确认等领域。更致力于为客户提供数据完整性保障(Data Integrity Assuance）的整体解决方案。我们已在全球45个国家，参与或主持了8，000多个项目。我们的客户包括全球知名跨国企业和地方领头企业。我们是山德士、特瓦等公司的全球服务伙伴，同时也与赛诺菲、辉瑞、罗氏、诺华等知名制药企业保持长期稳定合作关系。

PQE目前已进入中国市场，服务中国企业。我们期望能成为一个成本最优、品质最高的服务咨询公司。将秉承We Act Locally,Think Globally的商业理念。