Regulatory Affairs Manager
AbbVie
- Maidenhead, Berkshire
- Permanent
- Full-time
- Leading a team of Project Managers and Regulatory Affairs Specialists focused on the UK market.
- Managing all regulatory activities relating to licensing, regulatory changes, and submissions to MHRA.
- Contributing to a Brand Team representing Regulatory Affairs.
- Reviewing ABPI code including materials assessed, examined, or certified by a non-pharma final signatory.
- Leading continuous and process improvement projects.
- Hold a university degree in Pharmacy, Pharmacology, Biology or related disciplines.
- Have experience in a regulatory affairs position with a strong understanding of the UK market.
- Experience in line management or coaching is preferred.
- Have strong communication and coordination skills, and proficiency in communicating strategic and tactical issues to management.
- Demonstrate proven interpersonal skills and experience in working cross-functionally in a matrix organization.
- You should have the ability to influence upwards and get work done through people, irrespective of reporting relationships.