• 招聘类型：社招
• 工作性质：全职

职位描述

Primary Responsibilities

1. Responsible for the building, publishing, archiving activities and associated tasks for assigned Regulatory submissions within agreed timelines.

2. Adhering to quality control procedures and standards related to submission publishing.

3. Adhering to the appropriate use of document management systems, publishing and validation tools, through the use of working practices and quality control steps to ensure Regulatory compliance.

4. Support other team members with submission workload when necessary to provide flexible support for the submissions portfolio.

5. Support globallocal teams by completing tasks assigned by submission coordinators

6. Adhere to Pfizer compliance standards.

任职条件

Technical Skill Requirements

1. Computer literacy in MS WordOutlookExcelAdobe Acrobat.

2. Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards

3. Functional and technical knowledge and skills to do the job at a high level of accomplishment

Qualifications (i.e., preferred education, experience, attributes)

1. Proven technical aptitude

2. Quick learner with ability to multi-task

3. Ability to work with accuracy and attention to detail

4. Ability to work with autonomy andor part of a team in a busy environment

5. Demonstrated ability to work in a highly regulated environment

6. Demonstration of experience working in a customer service environment

职位要求

• 学历要求：本科及以上
• 工作经验：无
• 外语要求：英语

公司福利

• 电话补贴 
• 房补 
• 交通补贴