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Quality Lead(m/w/x)
Leading Quality Assurance for IFF project, ensuring GMP and BLA compliance. PhD-level qualification in Science strongly preferred. Company employee benefit programs.
Requirements
- Degree in Science, Pharmacy, or equivalent
- PhD-level qualification in Science strongly preferred
- Several years of industry experience in biopharma or related regulated industry
- Relevant experience in leadership quality positions
- Demonstrated leadership experience in quality role for capital investment program in PharmaBiotech
- In-depth knowledge of biologic product license application processes and regulatory requirements (FDA, Annex I, BLA)
- Strong understanding of pharmaceutical manufacturing processes, particularly large-scale biologics plants for bacterial processes
- Effective coaching skills for people development and performance improvement
- Visionary leadership to inspire quality culture across large, cross-functional teams
- Excellent communication and business partnering capabilities
- Expertise in Quality Risk Management, Quality Systems, and continuous improvement methodologies
- Strong interpersonal skills for multicultural, international environment
- Fluency in English required
- German and/or French highly advantageous
Tasks
- Lead Quality Assurance functions for IFF project
- Ensure compliance with Sanofi standards, GMP, BLA, and Annex I
- Develop and implement C&Q&V strategies and plans
- Manage DQ, SAT, FAT, IQ, OQ, and nP-PQ protocols
- Prepare final CQ reports and Validation Master Plan
- Serve as Quality focal point in Frankfurt
- Integrate quality requirements with Frankfurt Bio Campus
- Drive quality culture and GMP compliance performance
- Promote continuous improvement across all functions
- Manage proactive and reactive Quality Risk Management
- Represent project as primary quality escalation point
- Operate Quality Assurance, Quality Control, and Quality Systems
- Support Qualified Persons and Regulatory Affairs
- Develop and mentor IFF Quality team
- Manage IFF quality budget and schedule
- Optimize cost and schedule decisions
- Develop synergies with Frankfurt Bio Campus and Insulin Facility Beijing
- Contribute to digital transformation strategy
- Implement MES, batch review by exception, and SMART factory initiatives
- Communicate and escalate quality issues effectively
- Update and promote Sanofi Global Quality Documentation
- Maintain IFF GOPs and global procedures
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Native
- German – Basic
- French – Basic
Benefits
Corporate Discounts
- Company employee benefit programs
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Quality Lead(m/w/x)
Leading Quality Assurance for IFF project, ensuring GMP and BLA compliance. PhD-level qualification in Science strongly preferred. Company employee benefit programs.
Requirements
- Degree in Science, Pharmacy, or equivalent
- PhD-level qualification in Science strongly preferred
- Several years of industry experience in biopharma or related regulated industry
- Relevant experience in leadership quality positions
- Demonstrated leadership experience in quality role for capital investment program in PharmaBiotech
- In-depth knowledge of biologic product license application processes and regulatory requirements (FDA, Annex I, BLA)
- Strong understanding of pharmaceutical manufacturing processes, particularly large-scale biologics plants for bacterial processes
- Effective coaching skills for people development and performance improvement
- Visionary leadership to inspire quality culture across large, cross-functional teams
- Excellent communication and business partnering capabilities
- Expertise in Quality Risk Management, Quality Systems, and continuous improvement methodologies
- Strong interpersonal skills for multicultural, international environment
- Fluency in English required
- German and/or French highly advantageous
Tasks
- Lead Quality Assurance functions for IFF project
- Ensure compliance with Sanofi standards, GMP, BLA, and Annex I
- Develop and implement C&Q&V strategies and plans
- Manage DQ, SAT, FAT, IQ, OQ, and nP-PQ protocols
- Prepare final CQ reports and Validation Master Plan
- Serve as Quality focal point in Frankfurt
- Integrate quality requirements with Frankfurt Bio Campus
- Drive quality culture and GMP compliance performance
- Promote continuous improvement across all functions
- Manage proactive and reactive Quality Risk Management
- Represent project as primary quality escalation point
- Operate Quality Assurance, Quality Control, and Quality Systems
- Support Qualified Persons and Regulatory Affairs
- Develop and mentor IFF Quality team
- Manage IFF quality budget and schedule
- Optimize cost and schedule decisions
- Develop synergies with Frankfurt Bio Campus and Insulin Facility Beijing
- Contribute to digital transformation strategy
- Implement MES, batch review by exception, and SMART factory initiatives
- Communicate and escalate quality issues effectively
- Update and promote Sanofi Global Quality Documentation
- Maintain IFF GOPs and global procedures
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Native
- German – Basic
- French – Basic
Benefits
Corporate Discounts
- Company employee benefit programs
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Sanofi-Aventis Deutschland GmbH
Industry
Pharmaceuticals
Description
Das Unternehmen bietet Arzneimittel zur Prävention von Herz-Kreislauf-Erkrankungen an und setzt sich für die Verbesserung der Lebensqualität ein.
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