Global Supplier Quality & Compliance Manager (m / f / d) (Early Clinical Development) (m / w / d)

Our Company

At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company, we focus on long-term performance. We believe that, if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve; after all, we started with just 28 people. Now, we are powered by 50,000 employees globally who nurture a diverse, collaborative and inclusive culture.

Global Supplier Quality & Compliance Manager (m / f / d) (Early Clinical Development)

Vienna

JOB-ID : 27712

The position

Are you looking to grow your career in Quality Assurance within a cutting-edge pharmaceutical environment? We are currently seeking a talented and motivated Global Supplier Quality & Compliance Manager to join our Global Quality Medicine Department in Vienna. The role will focus primarily on suppliers performing Early Clinical Development / Phase I study activities.

In this role, you will be instrumental in advancing Boehringer Ingelheim's development pipeline by ensuring robust supplier quality systems and compliance standards. You will collaborate cross-functionally with global teams to oversee supplier qualification, oversight / governance and continuous improvement of our external partners, enabling the delivery of safe and effective medicines worldwide.

Join us and make a meaningful impact on global health through innovation and quality excellence.

Tasks & responsibilities

• Provide input into the global strategy for supplier quality management and ensure execution of the strategy for assigned suppliers and interact directly with the assigned suppliers (end to end quality management) to ensure appropriate supplier quality management and oversight
• Perform the process defined tasks of qualification, oversight and termination of suppliers for Quality Medicine, with a specific focus on suppliers performing Early Clinical Development / Phase I study activities
• Support the preparation, management, and the performance of the inspections with respect to the supplier related activities
• Provide consultancy and guidance cross-functionally on GxP topics regarding supplier and service-related topics and author the Quality Management Agreements, when required

Requirements

Please note that employment takes place via one of our external partners. The employment takes place exclusively at Boehringer Ingelheim RCV GmbH & Co KG.

Your Benefits

The remuneration for this position starts at EUR 74.000 gross annual target salary per year (full time). The actual salary package depends on professional experience and qualifications. We will be happy to discuss further details in person.

We are looking forward to receiving your application online!

By uploading your application documents via our application portal, we can treat your data confidentially and in compliance with the GDPR.

Do you have any additional questions about the position? Your HR Recruiting Manager for this position is Aleksandra Dawid.

On our career site you will find further information about Boehringer Ingelheim as an employer as well as information about the application process and our different departments.

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