Specialist Global QA Data Governance

BioNTech AG

Job

In this role, you will support the implementation of SAP Quality processes by training users, coordinating tests, and acting as a liaison between Quality and IT to ensure reliable data quality and governance.

Job summary

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Job technologies

Your role in the team

  • In this role, you will help ensure the effective and compliant use of SAP Quality processes that support BioNTech's commercial activities.
  • As the SAP Quality Key User, you will provide specialist expertise, support and training to end users, coordinate user acceptance testing, and act as a key link between Quality functions and SAP IT.
  • You will serve as the SAP Quality Key User, providing subject matter expertise on SAP Quality processes and Quality master data.
  • As a first point of contact for business users, you will help resolve questions and promote effective system use.
  • You will support reliable data quality and governance for commercial operations, facilitate Master Data uploads in electronic systems such as SAP and Veeva, and act as Data Steward for Quality Master Data.
  • You will develop, maintain and deliver SAP Quality training and user guidance.
  • By supporting users across the organization, you will help ensure consistent process execution, strong system adoption and the capabilities needed to use the system effectively.
  • You will coordinate and carry out user acceptance testing for system changes and enhancements.
  • This includes preparing and documenting test activities, supporting the resolution of issues, and confirming that business requirements are met before changes are deployed.
  • You will act as the interface between Quality stakeholders, Business Process Owners and SAP IT.
  • By facilitating communication, clarifying requirements and coordinating issue management, you will help drive the implementation of system improvements.

Our expectations of you

Education

  • You hold a degree in pharmacy, chemistry, biology, or a related scientific field, or an equivalent industrial qualification and experience.

Qualifications

  • You are well-versed in pharmaceutical compliance regulations and understand how to apply them in a system and process context.
  • You communicate and collaborate effectively with stakeholders across functions and are comfortable working in a multicultural environment.
  • You are detail-oriented and proactive, with a strong ability to create and manage quality-related documentation effectively.
  • You are fluent in English, and proficiency in German is considered a plus.

Experience

  • You have at least three years of experience in Quality Assurance and a strong background in computerized system projects.

What we offer

  • Your flexibility: flexible working hours | vacation allowance
  • Your growth: Digital Learning | Performance & talent development | Leadership development | Apprenticeships | LinkedIn Learning
  • Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape and make an impact | Support to reach your full potential
  • Your health and lifestyle: Company bike
  • Your mobility: Job ticket | Deutschlandticket
  • Your life phases: Employer-funded pension | Childcare

Benefits

Topics you will work on

Job locations

Map of the job locations
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  • Location Mainz
    Rheinland-Pfalz, Germany

About your employer

BioNTech is a cutting-edge immunotherapy company that is leading the way in developing new treatments for cancer, infectious diseases, and rare conditions. The company combines immunology research, modern therapeutic platforms, and bioinformatics tools to quickly develop new biopharmaceuticals.

Company size
250+ Employees
Founding year
2008
Company type
Established Company
Work model
Onsite, Hybrid
Industry
Pharmaceutical Sector, Chemical Industry, Biotech
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Specialist Global QA Data Governance

BioNTech AG