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≈ $51k – $111k per year (Estimated)
Location
In office (Mainz)

Confirmed on the employer's own hiring board on Oct 16, 2026. First seen by Alion on Oct 16, 2026.

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BioNTech is a German biotechnology company founded in Mainz in 2008 by the physician-scientists Ugur Sahin and Ozlem Tureci to develop individualised cancer immunotherapies using messenger RNA. Its mRNA platform, refined over a decade on oncology programmes, was redirected in early 2020 to produce Comirnaty with Pfizer, the first COVID-19 vaccine authorised in the West and the source of tens of billions of euros in revenue. The company has reinvested that windfall into its original mission, running a broad clinical pipeline of mRNA cancer vaccines, individualised neoantigen therapies and bispecific antibodies including the closely watched BNT327 programme.

Mainz, Germany | full time | Job ID: 11846

About the role:

The Manager Global Quality Systems - Data Governance position is critical for ensuring quality oversight in both local and global projects. This role ensures GxP compliance, effective Data governance and management, Data Integrity, risk-based decision making, and successful implementation of system and process changes.

Your Contribution:

  • You will provide Quality oversight for global and local computerized systems related projects, ensuring GxP compliance, appropriate data and process governance, and integration of quality requirements throughout the system lifecycle
  • You will act as QA approver and key Quality contact for system-related deviations, changes, business process documents, and Quality master data, ensuring compliant and risk-based decisions and processes
  • You will lead Quality-related projects or sub-projects, representing Quality requirements, driving implementation activities, managing stakeholders, and supporting successful deployment of computerized systems
  • You will coordinate and facilitate testing activities in quality related processes, especially in user acceptance testing
  • You will ensure data integrity, Quality data lifecycle management, and alignment with business and compliance requirements
  • You will facilitate risk assessments for Quality processes and ensure testing documentation adequately demonstrates intended use and compliance

A Good Match:

  • You hold a degree in pharmacy, chemistry, biology, or a related scientific field, or equivalent industrial qualification and experience
  • Several years (3+) of experience in Quality Assurance and a strong background as Business Lead in computerized systems related projects, with experience in local and global project environments
  • You are well-versed in pharmaceutical compliance regulations
  • You possess excellent communication and collaboration skills, enabling you to act as a bridge between IT and business stakeholders
  • 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

Your Benefits:

It's our priority to support you:

  • Your flexibility: flexible hours | vacation account
  • 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 & impact | Support for your full potential
  • Your health and lifestyle: Company bike
  • Your mobility: Job ticket | Deutschlandticket
  • Your life phases: Employer-funded pension | Childcare

Apply now - We look forward to your application!

Apply to our Mainz, Germanylocation by sending us your documents via our online form. For any questions, contact our talent acquisition team on: + 49 (0) 6131-9084-1291 (Monday-Friday from 1 PM to 3 PM CET).

Job ID 11846 (please always specify if you have any questions)

By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter.

Note for applications within Europe: Please note that if you wish to claim travel expenses incurred in connection with an in-person interview, we are obliged to carry out a sanctions list check*. This is carried out by our partner, HireRight. Travel expenses will only be reimbursed if this sanctions list check does not yield any matches. Reimbursement can be made provided that the check is successfully completed.

* Your first name, surname and date of birth will be processed for the sanctions list check. The legal basis for carrying out the sanctions list check for positions at BioNTech in Europe is BioNTech’s legitimate interest. Please note that BioNTech will not carry out the sanctions list check if no travel expenses are to be reimbursed. If you do not give BioNTech your consent to the sanctions list check, your travel expenses cannot be reimbursed. This will not affect your application.

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