Boehringer Ingelheim
Manager RA(m/w/x)
Part-timeTemporary contractOn-siteExperienced
Ingelheim am Rhein
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Boehringer Ingelheim(Senior) Manager RA(m/w/x)
Ingelheim am Rhein
Part-timeOn-siteExperienced
Description
You will drive the global lifecycle of veterinary medicines by defining CMC strategies and managing regulatory dossiers while acting as a key liaison between the organization and international authorities.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Master’s or university degree in Life Sciences
- •Initial experience in Regulatory Affairs or development
- •Understanding of pharmaceutical veterinary regulatory requirements
- •Excellent communication, negotiation and interpersonal skills
- •Excellent command of English
- •Experience in Regulatory Affairs or comparable roles
- •Knowledge of veterinary medicinal product requirements
- •Awareness of industry trends and competitors
- •High initiative and strong organizational skills
Education
Master's degree
OR
Bachelor's degree
Tasks
- •Define CMC regulatory requirements for assigned initiatives
- •Represent the RA CMC function in cross-functional teams
- •Serve as the central contact for technical and regulatory stakeholders
- •Oversee geographical expansion activities for veterinary products
- •Manage regulatory activities from submission to procedure completion
- •Liaise with the EMA and national competent authorities
- •Prepare and review quality-related documentation for dossiers
- •Support regional and local teams with product registrations
- •Develop and implement global regulatory strategies
- •Update and maintain regulatory tools and databases
- •Lead or support internal infrastructure projects
- •Engage proactively with regulatory authorities and external partners
Languages
English – Business Fluent
Benefits
Flexible Working
- •Hybrid work setup
Informal Culture
- •International and crossfunctional environment
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Boehringer Ingelheim and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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BO
Boehringer Ingelheim(Senior) Manager RA(m/w/x)
Ingelheim am Rhein
Part-timeOn-siteExperienced
New Job?Nejo!
The AI Job Search Engine
Description
You will drive the global lifecycle of veterinary medicines by defining CMC strategies and managing regulatory dossiers while acting as a key liaison between the organization and international authorities.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Master’s or university degree in Life Sciences
- •Initial experience in Regulatory Affairs or development
- •Understanding of pharmaceutical veterinary regulatory requirements
- •Excellent communication, negotiation and interpersonal skills
- •Excellent command of English
- •Experience in Regulatory Affairs or comparable roles
- •Knowledge of veterinary medicinal product requirements
- •Awareness of industry trends and competitors
- •High initiative and strong organizational skills
Education
Master's degree
OR
Bachelor's degree
Tasks
- •Define CMC regulatory requirements for assigned initiatives
- •Represent the RA CMC function in cross-functional teams
- •Serve as the central contact for technical and regulatory stakeholders
- •Oversee geographical expansion activities for veterinary products
- •Manage regulatory activities from submission to procedure completion
- •Liaise with the EMA and national competent authorities
- •Prepare and review quality-related documentation for dossiers
- •Support regional and local teams with product registrations
- •Develop and implement global regulatory strategies
- •Update and maintain regulatory tools and databases
- •Lead or support internal infrastructure projects
- •Engage proactively with regulatory authorities and external partners
Languages
English – Business Fluent
Benefits
Flexible Working
- •Hybrid work setup
Informal Culture
- •International and crossfunctional environment
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Boehringer Ingelheim and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Boehringer Ingelheim
Industry
Pharmaceuticals
Description
The company is focused on delivering lasting value to patients through innovative therapies and early clinical development.
Not a perfect match?
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