Boehringer Ingelheim sucht eine/n

RA Service Center - Manager

Ingelheim am Rhein, Germany

The Position

In this impactful role, you will play a key part in shaping the global regulatory strategy for a broad portfolio of veterinary products. Acting as a central interface between internal teams and external partners, you will drive the setup and continuous development of an international outsourcing program while ensuring the highest quality and compliance standards. Working closely with colleagues across the globe, you will take on a pivotal role in a dynamic and highly interconnected environment at Boehringer Ingelheim Vetmedica.

This position is limited until 31.07.2027

This position is part time eligible with 50%.

Tasks & responsibilities

In your new role you will take responsibility for the RA Outsourcing program for global veterinary products/product families. This implies a close collaboration with the RA Senior Managers according to our corporate strategy.
You will provide key support in setting up the outsourcing program. This includes conducting satisfaction surveys and evaluations of the quality of out-licensed activities (quality, safety and efficacy part, international tasks, database activities (BIRDS, DAVID)) with global scope. This includes overseeing related maintenance activities on a global scale as well as dossiers for geographic expansion. Evaluating regulatory initiatives and legislative changes in terms of relevance to the out-licensed product portfolio is also part of your job.
Another area of responsibility is the follow-up of global vendor management activities in coordination with the RA Senior Managers and the Head of RA Service Center.
You will check invoices for content accuracy and support budget planning.
In addition, you will be responsible for the management of external partners within the outsourcing program, i.e. you will act as an interface for all process-related and regulatory issues regarding the out-licensed product portfolio (over 100 pharmaceuticals and vaccines worldwide) between external service providers and BI RA technical teams.
Finally, you will initiate or support infrastructure projects assigned to you.

Requirements

Licensed pharmacist, alternatively veterinarian or biologist with master's degree
Several years of experience in international regulatory affairs with a sound understanding of international regulatory processes and procedures
Expertise in regulatory requirements for the approval of veterinary medicinal products in the EU; European approval procedures (CP, DCP, MRP), non-EU procedures
Excellent communication skills, cross-cultural mindset (especially for US, F, local OPUs) and understanding of processes and stakeholders in the BIAH
Experience in vendor management and oversight
Diplomacy in mediation and negotiations
Strategic and solution-oriented mindset
Willingness to travel on a small scale

As part of our commitment to transparency and fairness, salary information will be shared during the recruitment process. We also offer a comprehensive benefits and wellbeing package.

Applications from persons with severe disabilities are warmly welcomed. In cases of equal qualifications, such applicants will be given preferential consideration in the selection process.

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 appliation - The job posting is presumably online until July 24th, 2026. We reserve the right to take the posting offline beforehand.
Step 2: Virtual meeting in July
Step 3: On-site interviews in July/August

Abonnieren Sie Pharma-Jobbenachrichtigungen