As a Manager Global Quality Assurance CSV, you will support the validation of global computerized system in the BioNTech network and oversee pharmaceutical quality system processes for corporate GxP-critical applications, IT infrastructure, and projects.
Requirements
- Degree in pharmacy, chemistry, biology, or a related scientific field, or equivalent industrial qualification and experience
- At least 3 years of experience in Quality Assurance, particularly in Computer System Validation (CSV) / Computer System Assurance (CSA) and Data Integrity
- Solid understanding of GxP regulations and pharmaceutical quality systems, with experience in global and local project environments
- Hands-on experience in validation of systems like SAP, Laboratory Information Sysmtems (LIMS), and Manufacturing Execution Systems (MES)
- First audit experience and strong analytical and proactive capabilities, as well as strong problem-solving skills to effectively drive quality improvements
Benefits
- Flexible hours
- Vacation account
- Digital Learning
- Performance & talent development
- Leadership development
- Apprenticeships
- LinkedIn Learning
- Company bike
- Job ticket
- Deutschlandticket
- Employer-funded pension
- Childcare