Search the 4 jobs at Ipsen

As a Senior Quality Specialist, you will manage QMS processes, oversee Quality Risk Management, conduct internal and external audits, engage with supply chain colleagues, and ensure compliance with GxP standards. You will also support training initiatives and participate in regulatory inspections.

The Key Account Manager will focus on differentiating Ipsen’s product offerings to optimize patient care, engage stakeholders, and drive change within the healthcare system. Responsibilities include building relationships with healthcare professionals, utilizing business analytics for planning, and leveraging digital resources to support sales efforts.

The Principal Statistical Programmer will lead statistical programming activities for clinical trial data analysis and reporting, ensuring quality and compliance with regulatory standards. Responsibilities include collaborating with various teams, conducting quality control checks, and managing multiple projects. The role requires a strong background in SAS programming, regulatory submissions, and clinical trial data management.

The MS&T Analytical Manager at Ipsen Biopharm Ltd is responsible for overseeing analytical activities related to oral solid dose products, including method development, validation, and regulatory submissions. The role entails collaboration with cross-functional teams and CMOs, project management, and coaching team members. The manager will apply statistical methods for data analysis and ensure compliance with regulatory guidelines.