Regulatory Affairs and Quality Manager
- Employer
- Vita
- Location
- Basingstoke, Hampshire, UK
- Salary
- Competitive
- Start date
- 11 Jun 2021
- Closing date
- 11 Jul 2021
View more
- Discipline
- Quality, Regulatory Affairs
- Hours
- Part Time
- Contract Type
- Permanent
- Experience Level
- Management
Vita primarily develops, manufactures and markets veterinary medicines for honeybee health and we are recognized as the world leader in this niche sector. However, we also have non-veterinary products and others in development outside the scope of honeybee health. We are a small and dynamic team expanding our business internationally.
We are looking for an experienced Regulatory Affairs and Quality Manager, to deal with all aspects of registration and regulatory support of niche veterinary medicines, as well as other products. Experience of GMP and Quality systems would also be useful for this role.
The major tasks in regulatory affairs include the generation and compilation of data and product dossiers in accordance with European and other country-specific regulations; organisation of databases and application for registration, renewal and variation where appropriate. Preparation and maintenance of product labelling and literature. The post holder will eventually be expected to work largely on his/her own initiative, within a small team, liaising with country-specific distributors and regulatory bodies.
Experience with pharmacovigilance would be helpful, as the post holder will be involved with the veterinary pharmacovigilance system. This is currently a full-time position, based at our offices in Basingstoke, Hampshire.
However, it is possible that part-time working could also be considered.
Get job alerts
Create a job alert and receive personalised job recommendations straight to your inbox.
Create alert