BioNTech SE
Manager QA Compliance(m/w/x)
Full-timeOn-siteSenior
Mainz
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BIBioNTech SE
Executive Director Manufacturing Network QA(m/w/x)
Mainz
Full-timeOn-siteSenior
Nejo AI Summary
Leading GxP compliance for global pharmaceutical production sites at a medication developer. Extensive GxP compliance experience for pharmaceutical production sites and product launches required. Flexible hours, vacation account.
Requirements
- Degree in Life Sciences, Pharmacy, Chemistry, Engineering, or related field
- Advanced degrees (e.g., MSc, PhD, MBA) highly desirable
- Extensive experience in Quality Assurance, GxP compliance, and manufacturing operations within the pharmaceutical industry
- Significant experience in steering external manufacturing networks
- Demonstrated success in preparing and executing commercial product launches from a Quality Assurance perspective
- Familiarity with international regulatory landscapes and manufacturing operations
- Strong leadership capabilities
- Exceptional analytical and problem-solving skills
- Excellent communication and interpersonal skills
Tasks
- Provide strategic leadership for GxP-compliant global manufacturing operations
- Drive changes across sites while ensuring quality health and compliance
- Guide escalation and remediation activities within the manufacturing network
- Lead site-specific compliance to meet regional and global standards
- Represent Quality Assurance in key internal and external decision forums
- Prepare for forums to contribute effectively to strategic decision-making
- Lead a team of Site Quality Heads and Quality Assurance professionals
- Foster a culture of collaboration, accountability, and excellence
- Equip the team with necessary skills and resources for continuous improvement
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Flexible hours
More Vacation Days
- Vacation account
Learning & Development
- Digital learning
- Apprenticeships
- LinkedIn learning
Career Advancement
- Performance & talent development
- Leadership development
Other Benefits
- Your voice at the table
- Support for your full potential
Informal Culture
- Culture on an equal footing
Purpose-Driven Work
- Opportunities to shape & impact
Company Bike
- Company bike
Public Transport Subsidies
- Job ticket
- Deutschlandticket
Retirement Plans
- Employer-funded pension
Childcare
- Childcare
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of BioNTech SE and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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BIBioNTech SE
Executive Director Manufacturing Network QA(m/w/x)
Mainz
Full-timeOn-siteSenior
Nejo AI Summary
Leading GxP compliance for global pharmaceutical production sites at a medication developer. Extensive GxP compliance experience for pharmaceutical production sites and product launches required. Flexible hours, vacation account.
Requirements
- Degree in Life Sciences, Pharmacy, Chemistry, Engineering, or related field
- Advanced degrees (e.g., MSc, PhD, MBA) highly desirable
- Extensive experience in Quality Assurance, GxP compliance, and manufacturing operations within the pharmaceutical industry
- Significant experience in steering external manufacturing networks
- Demonstrated success in preparing and executing commercial product launches from a Quality Assurance perspective
- Familiarity with international regulatory landscapes and manufacturing operations
- Strong leadership capabilities
- Exceptional analytical and problem-solving skills
- Excellent communication and interpersonal skills
Tasks
- Provide strategic leadership for GxP-compliant global manufacturing operations
- Drive changes across sites while ensuring quality health and compliance
- Guide escalation and remediation activities within the manufacturing network
- Lead site-specific compliance to meet regional and global standards
- Represent Quality Assurance in key internal and external decision forums
- Prepare for forums to contribute effectively to strategic decision-making
- Lead a team of Site Quality Heads and Quality Assurance professionals
- Foster a culture of collaboration, accountability, and excellence
- Equip the team with necessary skills and resources for continuous improvement
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Flexible hours
More Vacation Days
- Vacation account
Learning & Development
- Digital learning
- Apprenticeships
- LinkedIn learning
Career Advancement
- Performance & talent development
- Leadership development
Other Benefits
- Your voice at the table
- Support for your full potential
Informal Culture
- Culture on an equal footing
Purpose-Driven Work
- Opportunities to shape & impact
Company Bike
- Company bike
Public Transport Subsidies
- Job ticket
- Deutschlandticket
Retirement Plans
- Employer-funded pension
Childcare
- Childcare
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of BioNTech SE and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
BioNTech SE
Industry
Pharmaceuticals
Description
Das Unternehmen entwickelt bahnbrechende Medikamente zur Verbesserung der globalen Gesundheit und zur Bekämpfung von Krankheiten.
Not a perfect match?
- BioNTech SE
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Full-timeOn-siteExperiencedMainz