Head of Pharmacovigilance Before you apply -Turn on alerts for jobs like this!
Veterinary Medicines Directorate, New Haw, Surrey
Head of Pharmacovigilance Before you apply -Turn on alerts for jobs like this!
Salary not available. View on company website.
Veterinary Medicines Directorate, New Haw, Surrey
- Full time
- Permanent
- Onsite working
Posted today, 30 Oct | Get your application in now to be one of the first to apply.
Closing date: Closing date not specified
job Ref: 4aeb5cffdcf345d88cab093248bd850b
Full Job Description
The Veterinary Medicines Directorate (VMD) is an Executive Agency of the Department for Environment, Food and Rural Affairs (Defra) and is responsible for ensuring the safety, quality, and efficacy of veterinary medicines in the UK. We have a vacancy for the Head of Pharmacovigilance This exciting and interesting post puts you at the heart of the Veterinary Medicines Directorate's (VMD) role in being the regulatory and policy lead responsible for issues concerning the authorisation, use, and manufacture of veterinary medicines in the UK. The VMD's aim is to protect public health, animal health, and the environment, and promote animal welfare by assuring the safety, quality and effectiveness of veterinary medicines. As Head of Pharmacovigilance, you will be responsible for the post-authorisation surveillance of veterinary medicines through the collation of suspected adverse event reports among other mechanisms. Veterinary medicines regulation has undergone a period of significant change due to the introduction of new legislation in Great Britain (GB), and the continued adjustment to the new landscape following Brexit with veterinary medicines regulation operating slightly differently in Northern Ireland (NI). This adds to the complexity of the work dealt with by the VMD.
Degree in veterinary science Memberships Must be eligible to be a member of the RCVS Experience required: You must have a good understanding and relevant experience in, or a demonstrable ability to get up to speed rapidly, in the regulation of medicinal products, the legislative process, and Pharmacovigilance and the wider regulatory environment. We're looking for you to have experience of / in:
- developing and leading a team
- developing business relationships
- providing strategic leadership
- leading change
- management of key business processes subject to demanding deadlines and managing conflicting priorities
- providing advice on complex issues in a way that is easy to understand. We're looking for someone that:
- Is a good communicator, both orally and in writing.
- Is proactive, working on your own initiative using a variety of media to communicate messages and reporting progress against strategic objectives or targeted outcomes.
- Is proficient in the use of Microsoft Office 365 packages, particularly Microsoft Teams, Word, Excel, PowerPoint, and Outlook, and can learn in-house packages quickly.