As a Qualified Person at Vectura, you’ll find yourself in a position with lots of variety, supported by a small, friendly team.
The work our Quality team does is crucial to ensuring our products are manufactured in accordance with industry standards, regulatory requirements as well as Vectura and customer requirements.
As a named QP you will be responsible for the sign-off of client clinical product manufactured onsite for trials.
This role isn’t just restricted to batch sign-off though, so you’ll have the opportunity to utilise your experience to the fullest.
Other key tasks involve, but are not limited to:
Supporting a range of cross-functional development projects as the Quality representative
Supporting large infrastructure development projects
Chairing Quality Management Reviews
Leading supplier and internal audits
Training, coaching, and mentoring members of the quality team and broader Vectura staff
Supporting the development of annual budgets
What you need
You will be eligible to act as a Qualified Person in accordance with SI 2004:1031 and SI 2012:1916 and will have worked in an IMP environment.
You will have a good level of experience at operating in a senior role, with the flexibility to adapt and a willingness to adapt to take on new challenges
Experience of working with inhaled medicines would be highly desirable, but not essential. Experience in working with medical devices or combination products would also be desirable.
If you’re interested in a role with lots of variety, in a fast-paced and expanding work environment we’d love to hear from you. Apply today to find out more.