Clinical Supply Associate
External
Onepartnergroup Väst Ab · Göteborg, Västra Götalands LänPrepare for this interview
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Responsibilities
- The CSA supports Clinical Supply Management with task-based activities that include:
- Documentation and coordination Product Quality Complaints
- Coordination of Product Quality Sample Returns.
- Documentation and facilitation of Deviations affecting product quality or regulatory compliance.
- Management of documents in the electronic Trial Master File and quality control
- Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards.
- User Acceptance Testing
- Utilising Supply Chain Management systems to support agile ways of working.
- Continually improving the Clinical Supply Chain processes through visual management, problem solving, global standardisation and process confirmation.
Additional Information
Join us in Pharmaceutical Technology and Development (PT&D) where we transform innovative science into actual medicines that help millions of people globally. As a Clinical Supply Associate (CSA), you will support the Clinical Supply Chain Management team in delivering clinical material and associated information to meet agreed clinical demand. This role is perfect for those who thrive in a task-based, agile, and global environment. You will have the opportunity to develop leadership skills and enterprise acumen, becoming a super-user and leading improvement initiatives within a year. This role is a great opportunity for someone pursuing a career within Clinical Supply/Quality Management
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