Clinical Quality Manager

Main requirements are:

• Broad experience in different clinical trials stages/areas (at least 5 years), preferably also in Quality Assurance related activities
• Experience in participation and preparation to audits and inspections (preferable experience in FDA/EMA inspections etc.)
• Deep knowledge of the Clinical Quality System scope and structure/international standards, regulations and requirements/ GCP/GMP/GDP/other relevant GxP guidelines
• Understanding of the role of Quality Manager and requirements
• Ability to find out gaps and issues and develop effective CAPA on that

• Experience in working in international initiatives, networking with colleagues from other countries
• Excellent presentation skills and communication with senior leaders
• Fluent level of English

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.