Manager Global QA Data Governance
BioNTech Mainz, Rhineland-Palatinate, Germany
Biotechnology Research · 1,001-5,000 employees
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About the role
The role involves providing quality oversight for global and local computerized systems to ensure GxP compliance and effective data governance. You will act as a key quality contact for system-related deviations, changes, and risk assessments while leading quality-related projects.
What they look for
Requirements
Candidates must hold a degree in a scientific field such as pharmacy, chemistry, or biology, along with at least three years of experience in quality assurance. Strong knowledge of pharmaceutical compliance regulations and experience in computerized systems project environments are required.
Benefits
Full description
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, 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 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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