Regulatory Affairs Consultant - Labelling
Germany, Remote Additional Locations: Switzerland, Remote 职位编号 R0000039108 类别 Consulting关于这个职位
We are seeking an experiencedRegulatory Affairs Consultantspecializing 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:
Manageend-to-end labeling lifecycleincluding preliminary assessment, implementation, and post-approval maintenance
Provide innovation and technical expertise for the creation, maintenance, and implementation of labeling to meetcountry-specific regulatory requirements
Execute labeling operations globally with precision and efficiency
Participate in a'follow the sun' modelto 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 yearsof experience in the biotech/pharmaceutical industry
Labelling/regulatory experiencewith 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 amatrix organizationis expected
Ability to work effectively in a global, virtual team environment
Fluent in German and English, written and spoken
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