(Senior) Manager RA

The Position  

Join our Global Regulatory Affairs (RA) team in Germany as a (Senior) RA Manager and take on global responsibility for the qualityrelated components of regulatory dossiers for pharmaceutical veterinary medicinal products. 
Look forward to an exciting role in an international, crossfunctional environment with regular interactions across countries and regions. Actively contribute to the development, registration and lifecycle management of products with significant business impact – across all therapeutic modalities. 

This position has a hybrid setup with approximately 3 days per week on site.  

This position can be filled either as RA Manager or Senior RA Manager.  

This position is limited for 12 months.  

This position is part time eligible with 80 %.  

Tasks & responsibilities  

• Drawing on your knowledge of EU and key market pharmaceutical regulations, you will define CMC regulatory requirements for assigned initiatives and represent the RA CMC function. 
• Acting as RA CMC Product Manager, you will serve as the central contact point for internal and external stakeholders on technical or regulatory aspects throughout the lifecycle of an assigned product. 
• In addition, you will oversee geographical expansion activities (geo expansions). 
• As Manager for global pharmaceutical veterinary medicinal products, you will be responsible for regulatory activities from submission to completion of procedures during the lifecycle of an assigned product. 
• You will act as a key contact for the EMA as well as national competent authorities within European regulatory procedures.  

Additional tasks for the Senior RA Manager role 

• You will prepare, review and deliver quality‑related documentation for new submissions and lifecycle management of pharmaceutical veterinary medicinal products. 
• By providing the required documentation, you will ensure effective support and coordination of regional and local RA teams in product registrations. 
• Leveraging your expertise, you will develop and implement sound regulatory strategies for your assigned products. 
• Your responsibilities will include updating and maintaining regulatory tools and databases, as well as taking on leadership or support roles in infrastructure projects. 
• Through proactive engagement with regulatory authorities and external partners, you will position Boehringer Ingelheim as a trusted and innovative partner. 

Requirements  

• Master’s degree or university degree in Life Sciences (e.g., Pharmacy) 
• Initial experience in Regulatory Affairs and/or pharmaceutical product development 
• Strong understanding of regulatory requirements for pharmaceutical veterinary medicinal products and global regulatory processes is an advantage 
• Excellent communication, negotiation and interpersonal skills 
• Excellent command of written and spoken English  

Additional requirements for Senior RA Manager  

• Several years of experience in Regulatory Affairs or comparable roles within the pharmaceutical industry, including interactions with regulatory authorities and leading RA sub‑teams 
• Strong knowledge of regulatory requirements for veterinary medicinal products and global regulatory processes 
• Awareness of industry trends and competitor activities 
• High level of initiative, strong organizational skills and proven ability to manage complex portfolios in diverse environments 

Ready to contact us?   

If you have any questions about the job posting or process - please contact our HR Direct Team, Tel: +49 (0) 6132 77-3330 or via mail: hr.de@boehringer-ingelheim.com  

Recruitment process: 
Step 1: Online application - The job posting is presumably online until February 26th, 2026. We reserve the right to take the posting offline beforehand. Applications up to February 19th, 2026 are guaranteed to be considered.  
Step 2: Virtual meeting in the period from mid February till beginning of March 
Step 3: On-site interviews mid of March