Associate Director Quality Assurance

1 mese fa


Rho, Lombardia, Italia Teva Pharmaceutical Industries A tempo pieno
About Us

Teva Pharmaceutical Industries is a leading international supplier of active pharmaceutical ingredients (APIs). With a broad portfolio of over 350 API products, we are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies.

Job Summary

We are seeking an experienced Associate Director Quality Assurance to ensure that a Quality Compliance System is in place at TAPI manufacturing sites and R&D centers, securing compliance of activities, quality risk management, escalation of risks, and continuous improvement.

Key Responsibilities
  1. Provide governance through strong collaboration with manufacturing site operations to foster excellence in inspection management and inspection readiness at TAPI sites.
  2. Interact across the matrixed organization specifically with TAPI's Global Quality Compliance, Manufacturing Science & Technology, Research & Development, Supply Chain Operations, Regulatory Affairs and other network manufacturing and supply sites.
  3. Ensure that each site receives the right level of support to maintain and enhance GMP compliance, to solve quality-related service issues, to identify areas of improvement for quality operational performance in line with business needs and in accordance to TAPI standards.
  4. Foster and develop onsite Quality culture across all TAPI sites.
Requirements
  • 15+ years of experience as a functional leader with technical, team management, and operational responsibility.
  • Continuous professional development.
  • Advanced practical knowledge of pharmaceuticals manufacturing and control, facility design, utilities, maintenance, and calibration.
  • Advanced knowledge of local current and upcoming legislation and current Quality best practices.
  • International experience is an advantage.
  • Advanced knowledge of cGMP requirements for products and process.
  • Advanced understanding and insight into the different aspects of quality functions like QC, QA, Quality Systems, Compliance, Documentation, etc.
Preferred Qualifications
  • Fundamental knowledge of MRP Systems and GMP impacting computer systems, like TrackWise TAPI, Priority, StarLIMS and software platforms typically used by TAPI.
  • Ability to understand and execute against TAPI Quality Management System.
  • Advanced knowledge of quality systems.
  • Advanced experience in working with matrix environment.
  • Advanced knowledge in Auditing and Problem Solving.
  • Expert communication skills – written and verbal and advanced team work skills.
What We Offer

Teva Pharmaceutical Industries is committed to equal opportunity in employment. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process.



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