Labeling Contractor - Zug, Schweiz - Barrington James
Beschreibung
Zug- JOB TYPE
- Contract
- EMP TYPE
- Full-Time
- EXPERTISE
- Regulatory Affairs
- SALARY TYPE
- Hourly
- SALARY
- Negotiable
Key Responsibilities:
- Management of product information texts and documents across Europe and International rollout
- Diligent review and amendments to ensure consistent quality and compliance with standards of labeling
- Anticipate and plan required labeling revisions and translations, with accountability for timing and quality of execution
- Creation of version management and tracking of labeling documents for approved medicinal products
- Support the development of an internal labeling management system
- Support creation of local packaging artworks
- Close coordination with the regional and global regulatory strategy, labeling, advertising and promotion teams
Experience required:
- B.S. or graduate degree in life sciences
- 13 years of Regulatory Affairs experience in drug development and/or product registration activities within the pharma/biotech industry
- Basic experience with global regulatory documents and requirements for medicinal products, including exposure to regulatory labeling
- Knowledge of several EU languages is beneficial
LI-Remote
Consultant
- Harriet Dunbar
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