Specialist Global QA Data Governance (Mainz, RP, DE, 55131)
Notify me about similar jobsAbout this opportunity
Mainz, Germany | full time | Job ID: 11847
About the role:
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.
Your Contribution:
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 like 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.
A Good Match:
You hold a degree in pharmacy, chemistry, biology, or a related scientific field, or equivalent industrial qualification and experience.
You have at least three years of experience in Quality Assurance and a strong background in computerized system projects.
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.
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, Germany location 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 11847 (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.
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1502 comparable Quality roles across 147 biopharma companies.
Salary context
261 of 1502 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1502 comparable roles
+ 48 more countries
Seniority mix
731 of 1502 peers have a known seniority level
Therapeutic area mix
3 of 1502 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Notify me about similar jobs
Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
Or follow a whole field: get every new Quality job in Germany, and choose locations and companies.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.