Global Director, Quality, Regulatory & Pharmacovigilance Operations & Compliance

We are seeking an experienced Global Director to oversee Quality, Regulatory, Pharmacovigilance Operations and Compliance activities.

You will be responsible for:

- Leading the global regulatory strategy, planning, and execution of lifecycle management activities for finished products and active substances, both for the core business and related projects.

- Leading interactions with Health Authorities throughout the product lifecycle, as well as with other relevant external stakeholders.

- Overseeing and assisting cross-functional projects impacting the QRAPV Area related to lifecycle management, operations, processes, and compliance, participating in and supporting project teams.

- Defining the regulatory compliance strategy within the QRAPV Area, leading the definition and execution of CAPA plans by the corresponding teams. 

- Work towards the continuous improvement of processes in the QRAPV Area, including the implementation of relevant systems/tools (together with the IT team), harmonization and standardization initiatives, and company projects focused on process improvement/efficiency, participating in and supporting the relevant project teams.

- Establishing the department's long-term strategic plan.

- Handling the department's financial forecasting, allocation of financial resources, and overall vision for the area.

If your skillset matches these responsibilities. Please apply below.