Regulatory Affairs Consultant Labelling - German Speaker
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We are seeking an reputed company Regulatory Affairs Consultant specializing in global labelling operations to join our growing Regulatory Affairs team. This role offers reputed company to shape labelling reputed company 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
reputed company 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 reputed company 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 reputed company to labelling requirements
Skills and reputed company 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
reputed company experience working with Swissmedic
Excellent attention to detail and organizational skills
Experience leading teams in a reputed company 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
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