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法规事务顾问(标签方向)- 德语

雇主

Parexel

地点

远程 · 瑞士

待遇

CHF面议

工作模式

远程

截止日期

12月6日

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岗位摘要

When our values align, there's no limit to what we can achieve.

岗位职责

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
We are seeking an experienced Regulatory Affairs Consultant specializing in global labelling operations to join our growing Regulatory Affairs team. This role offers the opportunity to shape labelling strategy across multiple markets and drive global alignment of product information for pharmaceutical portfolio of our clients.
The role can be fully home based or office based.
Key Responsibilities:
Manage end-to-end labeling lifecycle including preliminary assessment, implementation, and post-approval maintenance
Provide innovation and technical expertise for the creation, maintenance, and implementation of labeling to meet country-specific regulatory requirements
Execute labeling operations globally with precision and efficiency
Participate in a 'follow the sun' model to ensure timely execution of labelling activities across time zones
Prepare and review labelling documents for regulatory submissions and variations
Maintain labeling databases and tracking systems
Support global labelling harmonization initiatives
Collaborate with regional regulatory teams to ensure compliance with local requirements
Monitor regulatory intelligence related to labelling requirements
Skills and Experienced required for the role:
University degree in a life science discipline
A few years of experience in the biotech/pharmaceutical industry
Labelling/regulatory experience with global responsibilities
Experience with CCDS development and maintenance
Strong understanding of regulatory labelling requirements across multiple markets
Direct experience working with Swissmedic
Excellent attention to detail and organizational skills
Experience leading teams in a matrix organization is expected
Ability to work effectively in a global, virtual team environment
Fluent in German and English, written and spoken
Originally posted on Himalayas

申请条件

- University degree in a life science discipline
- A few years of experience in the biotech/pharmaceutical industry
- Labelling/regulatory experience with global responsibilities
- Experience with CCDS development and maintenance
- Strong understanding of global labelling regulations and country-specific requirements
- Proficiency in managing end-to-end labelling lifecycle processes
- Excellent organizational and project management skills
- Ability to work collaboratively across regional and cross-functional teams
- Strong attention to detail and accuracy in document preparation
- Effective communication skills for regulatory submissions and stakeholder coordination
- Familiarity with labelling databases and tracking systems
- Capability to work in a flexible, time-zone-spanning environment (e.g., follow-the-sun model)

雇主简介

Parexel is a global clinical research organization providing clinical trials, regulatory consulting, and market access services to improve world health.

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数据来源:Himalayas

岗位信息来源于公开渠道,版权归原作者所有