What are the responsibilities and job description for the R&D Compliance Expert position at Teva Pharmaceutical Industries?
Teva Pharmaceuticals is committed to equal opportunity in employment. We believe that diversity and inclusion are essential to our success and strive to create a workplace where everyone feels valued, respected, and empowered to contribute their best work. As a Senior Director of Quality R&D, you will be part of a team that is dedicated to making a positive impact in the lives of millions of people worldwide.
About the Company
Teva Pharmaceuticals is a leading manufacturer of generic medicines, producing many of the products on the World Health Organization's Essential Medicines List. We are proud to make a difference in the lives of millions of people worldwide.
- Leading and managing all quality activities in R&D, ensuring compliance with GLP, GCP, and CMC standards
- Developing and implementing quality strategies to drive innovation and continuous improvement in pharmaceutical development and manufacturing
- Ensuring inspection readiness and successful authority inspections
- Cross-functional collaboration with Operations, Commercial, R&D, RA, MS&T, Supply Chain, Engineering, Procurement, and more
