Associate Director Quality and Compliance
3 giorni fa
At Teva Pharmaceuticals, we are seeking an experienced Associate Director Quality and Compliance to join our team. As a key member of our Quality Assurance department, you will be responsible for ensuring that our manufacturing sites and R&D centers maintain a Quality Compliance System that meets regulatory requirements.
Key Responsibilities:
- Implement and maintain a Quality Risk Management system to identify and mitigate potential risks
- Support complex investigations at sites to ensure comprehensive and scientific investigations
- Prepare sites for successful Health Authority inspections
- Monitor and communicate regulatory actions and compliance risks
- Coordinate the implementation of Global Projects improving patient supply and quality compliance
- Lead and conduct best practice and knowledge sharing routine forum meetings
- Conduct data Integrity gap assessments at sites
- Participate in Human error reduction program
- Ensure CAPA implementations and effectiveness checks are executed timely at sites
Requirements:
- Bachelor's Degree in chemistry, microbiology, pharmacy, engineering, or related science-based degree
- Master's Degree preferred in science, business, healthcare, or an equivalent combination of education and experience related to Quality Assurance/Quality Control
- APIs Manufacturing / SME experience required
- 15+ years of experience as a functional leader with technical, team management, and operational responsibility
- Advanced practical knowledge of pharmaceuticals manufacturing and control
- Fluent in English
About Teva Pharmaceuticals:
Teva Pharmaceuticals is a leading international supplier of active pharmaceutical ingredients (APIs). We are committed to equal opportunity in employment and strive to create a diverse and inclusive work environment.
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