Senior Director​/Site Quality Head

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

The Site Quality Head provides strategic and operational leadership for all Quality functions across Manufacturing, Packaging, Importation, and Laboratory Operations. This role is accountable for fostering a strong quality culture, ensuring compliance with regulatory requirements, and maintaining the highest standards of product quality and patient safety.

• Development, implementation, and execution of quality procedures and standards
• Establishment Licensing compliance
• Quality on the Floor activities, audits, and batch disposition/release
• Management of laboratory investigations, deviations, complaints, and nonconformances
• CAPA development, implementation, and effectiveness monitoring
• Quality metrics, trending, and performance reporting
• Validation program compliance
• Oversight of equipment, facilities, and utility systems to ensure adherence to established quality requirements

The role is responsible for leading the development, standardization, implementation, monitoring, and continuous improvement of Quality Systems, compliance programs, industry best practices, and corporate quality initiatives. The successful candidate will drive proactive quality and compliance improvements while strengthening a culture of operational excellence and Good Manufacturing Practice (GMP) compliance.

This position also serves as the Senior Person In Charge (SPIC) for Controlled Drug Substances and Narcotics.

• Lead the site's Quality organization, including Quality Assurance, Quality Control, Microbiology, Quality Systems, and Quality Compliance.
• Ensure a robust and continuously improving Quality Management System (QMS) is maintained.
• Ensure products are manufactured, released, and distributed in compliance with cGMP requirements and approved regulatory specifications.
• Serve as the highest-ranking quality authority on site with independent decision-making responsibility regarding product quality and potential market actions.
• Assess, manage, and mitigate quality risks to ensure products are safe, effective, and compliant before reaching patients.
• Partner with business leaders to ensure a reliable and compliant supply of products.
• Develop, implement, and continuously improve the Site Quality Program in collaboration with the Site General Manager and Corporate Quality leadership.
• Oversee the collection, analysis, and communication of quality data and performance metrics to site leadership, Corporate Quality, and key internal and external stakeholders.
• Direct Quality Control laboratory operations, including analytical method transfers, testing, and approval or rejection of raw materials, packaging components, in-process materials, and finished products.
• Champion a sustainable culture of quality by promoting accountability, open communication, continuous improvement, and employee engagement.
• Build and maintain strong partnerships with the site leadership team and cross-functional stakeholders.
• Act as a strategic business partner to Supply Chain, Project Management, R&D, Manufacturing Sciences & Technology (MS&T), and Commercial teams to achieve business objectives and project milestones.
• Provide leadership and expert support during internal audits, customer inspections, and regulatory inspections.
• Ensure Quality KPIs meet established targets and that CAPA commitments are implemented on time, with effectiveness verified through ongoing monitoring.
• Develop, manage, and oversee the annual Quality Operations budget while optimizing resources and organizational effectiveness.
• Provide quality oversight for two pharmaceutical manufacturing sites located…