The position
As of now we are seeking a Global Quality Medicine Data Governance Manager. In this role you will leverage expertise in data and process integration and will be responsible to ensure the accuracy, usability, availability and security of data generated in the Quality Medicine department.
Tasks & responsibilities
* Step into a pivotal role where you will use your business process expertise to lead the resolution of complex Data Governance demands submitted by Key Stakeholders from across the company
* Triaging the demands, assembling the correct solution team and ensuring implementation for new or amended data structures to optimize Business Intelligence Reporting needs of customers
* Embrace the responsibility for development, maintenance and oversight of the processes, standards, and systems used in the implementation of Data Governance procedures according to the standards of the Data Governance office
* Become the driving force behind executing the Data Governance strategy including organizing and monitoring resources. Set and manage the priorities and timelines in alignment with the Head of the QM Data Governance Office
* Your meticulous attention to detail will ensure the integrity and accuracy of our data, contributing to the overall quality of our work and facilitating advanced reporting and analytics
Requirements
* PhD: 3 years' GxP experience within the pharmaceutical industry, CROs or regulatory authorities or MSc: 5 years' GxP experience within the pharmaceutical industry, CROs, or regulatory authorities
* Project Management Certification or 5 year's project management experience, demonstrating increasing complexity of projects managed
* Direct experience as a Management System, Process and/or Capability Lead
* Demonstrated leadership skills and knowledge of processes in quality management
* Excellent ability to present complicated content in a clear, comprehensible and target group-oriented manner, presentation confidence (in English)
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
* Flexible working time models : home office and flexible working hours, depending on department and position – many things are possible with us
* Additional days off ("bridge-days") : more free time through additional days off to bridge single working days between bank holidays and the weekend – without having to use vacation days
* Canteen & Cafeteria : whether it's coffee and croissant for breakfast, various lunch menus or snacks in between – our subsidized staff restaurant & cafeteria has something for every taste including vegetarian and vegan options
* Learning & development : diverse training and development opportunities for your personal and professional growth. Because: you never stop learning
* Health promotion : health is important to us – that's why we offer different programs to promote physical and mental health
* Public transport ticket : we encourage our employees to use public transport on their daily way to work. Costs for public transport? We cover them
The remuneration for this position starts at EUR 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 Katrin Spögler.
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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