Teva Pharmaceuticals
Senior Director, Site Quality Head(m/w/x)
Vollzeit
Senior
Keine Angabe
Ulm
TE
Teva Pharmaceuticals4 Tage
Head of Quality Manufacturing, EU, India & LATAM Solids & LCO cluster(m/w/x)
Vollzeit
Senior
Keine Angabe
Ulm
Nejo KI-Zusammenfassung
In this role, you will lead quality activities across multiple regions, ensuring compliance and product excellence. Your day-to-day responsibilities will include managing quality oversight, driving continuous improvement, and fostering a proactive quality culture while supporting a high-performing global team.
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Anforderungen
- •Minimum of 15 years in pharmaceutical manufacturing quality operations and leadership
- •Direct interaction with health authorities
- •Experience in large, complex matrixed environments with global processes
- •Practical knowledge of analytical techniques and microbiological principles
- •Product and technology transfer
- •Practical knowledge of Global Compliance and Regulatory requirements
- •Practical knowledge in manufacturing, testing and health authority inspections
- •Ability to develop and execute Strategic / Long Range and Annual Business Plans
- •Practical knowledge on risk management
- •OpEx and LMS knowledge
- •Strong critical thinking and problem-solving skills
- •Strong leadership and change management skills
Keine Angabe
Berufserfahrung
15 Jahre
Deine Aufgaben
- •Lead and manage quality activities in the cluster
- •Provide quality oversight for Teva manufacturing sites and suppliers
- •Ensure product quality and compliance with regulations
- •Secure timely development, manufacturing, and supply of products
- •Establish management infrastructure for quality-compliant decisions
- •Confirm inspection readiness through successful authority inspections
- •Drive proactive quality risk management processes
- •Foster a culture of continuous improvement and risk-based thinking
- •Lead offshoring centers for Stability Testing and PQR/APR Compilation
- •Guide Site Quality Heads in independent decision-making on product quality
- •Develop projects to simplify quality business processes
- •Drive tools of the Teva Lean Management System
- •Sponsor execution of strategic compliance initiatives
- •Build and manage infrastructure for quality relations with external suppliers
- •Ensure quality compliance secures supply for internal and external customers
- •Influence strategy related to quality function and compliance
- •Develop strategic plans with Quality Compliance to achieve quality goals
- •Support operations initiatives for gross margin improvement
- •Ensure continuous improvement of the Quality Management System (QMS)
- •Lead a compliant quality and manufacturing network
- •Implement and improve the Teva QMS at site level
- •Drive standardization and harmonization of best practices
- •Ensure sites are inspection-ready and manage inspection processes
- •Establish a strong deviation investigation management system
- •Support resolution of severe quality incidents
- •Foster identification and implementation of best practices and technologies
- •Develop and lead optimization and efficiency processes
- •Ensure knowledge management across the network
- •Oversee Stability Testing in offshore centers
- •Address product robustness and compliance issues
- •Coordinate testing, shipping, and storage of stability samples
- •Identify cost-saving opportunities in testing and resources
- •Ensure EHS&S mindset in quality operations and laboratories
- •Lead, mentor, and develop a high-performing global team
- •Support professional growth and selection of key quality resources
Sprachen
Englisch – verhandlungssicher
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