As drug safety specialist you're responsibilities will be based on your experience and knowledge of the regulatory standards and guidelines. Activities will mostly be focused around overseeing compliance activities such as performing pharmacovigilance audits and managing agreements regarding pharmacovigilance. Other activities will focus around managing third party supplier quality by writing safety documentation, coordinating updates and processing data.

The organisational goal is to create more accessible an affordable healthcare around the world. By optimizing production processes and continuously improving drug quality, they aim to reduce the cost of healthcare around the world. As drug safety specialist you'll become a part of the drug safety team, a small and close knit group of 10 employees, with different levels of experience en responsibilities. Given the responsibilities of the team include managing safety and quality in satellite facilities around the world and getting them all on the same level, you'll be in constant cooperation with your colleagues.