With deep pharmaceutical expertise, a strong understanding of global regulations and legislation, and exceptional attention to detail, Regulatory Affairs team manages everything from pre-market authorisation to post-marketing activities.
Their work enables Douglas to launch new products globally - and keep them safely and compliantly on the market - ensuring patients everywhere can access high-quality, trusted medicines.
We regularly recruit:
Regulatory Affairs Associates to develop and maintain pharmaceutical dossiers, securing product registrations and variation approvals. Compliance is critical at Douglas, and our RA Associates play a key role in making this happen.
Pharmacovigilance team members operate independently from Regulatory Affairs but play a crucial role within our overall quality system. This team is dedicated to patient safety, team monitoring and evaluating the safety of our medicines throughout their entire lifecycle. They collect, assess, and analyse data on potential side effects, ensuring any risks are identified and managed quickly and effectively.
We look for science or pharmacy-qualified team members with an understanding of the regulatory affairs environment, ideally with experience in the pharmaceutical sector, and a strong eye for detail, organisation, and quality.
