This is a leadership role with expectations aligned to the Leadership Capabilities and Behaviours as set out in the Abbott UK Employee Handbook
Job Summary
This is a leadership role with expectations aligned to the Leadership Capabilities and Behaviours as set out in the Abbott UK Employee Handbook.
To define, plan, coordinate and integrate regulatory activities associated with systems, processes and materials across Dundee, Oslo and San Diego.
Lead and participate in cross-functional project teams involved in business-critical initiatives (e.g., new product introduction, development projects, major design changes).
Matching Summary
This is a leadership role with expectations aligned to the Leadership Capabilities and Behaviours as set out in the Abbott UK Employee Handbook.
Skills & Requirements
Must-have
Project Management
Regulatory Strategy
Cross-Functional Leadership
Risk Management
Global IVD Regulations
Nice-to-have
Commercially aware
Pro-active compliance culture
Lessons learned culture
Best practices implementation
Key Requirements
Degree or equivalent
Experience in a regulated industry
History of managing projects
Knowledge of Project Management tools
Experience in product development or manufacturing in a medical device product