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注册副经理-北京(Contract)

单位:泰格医药类型:社招地点:北京市更新:2026-09-24

岗位信息

招聘单位泰格医药
工作地点北京市
官方更新时间2024-08-22T13:42:50

职位描述

Short role description:

RA Associate Manager is responsible for implementing regulatory strategy to obtain the regulatory approval to

support various development, responsible for delivering high standard product licenses lifecycle management for

the designated product group; to support line manager for regulatory intelligence collection and analysis,

integration for regulatory strategy assessment.

Typical Accountabilities:

• Implement regulatory strategies to achieve in-time and high quality approval and facilitate full speed launch.

• Maintain product licenses through timely lifecycle management with high standard.

• Effectively manage the local and global regulatory support systems/information to ensure good coordination

for all stakeholders.

• Establish relationship with local regulatory authorities with the guidance of senior regulatory manager.

• Monitor local regulatory environments and communicate to key stakeholders, support to exert regulatory

influence through company initiatives and/or industry association joint forces.

任职要求

• Bachelor degree or above in Pharmacy, Medical,Biology or related field.China Pharmacist/Physician License is plus • Minimum 2 years’ experience in below position.Minimum 4 years working experience in regulatory affairs of MNC Ph

arma Company.

• Understand the current regulatory practices and regulation in China.

• Strong collaboration across teams.

• Fluent in both oral and written English.

• Good project management skill.

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