Lead a team within Veterinary Sciences, managing high-volume regulatory applications and overseeing key projects in a fast-paced environment. This is an initial 2-year contract with strong potential to become permanent.
Key Responsibilities:
* Manage regulatory applications (variations, new applications, transfers, scientific advice, SPC harmonisation).
* Act as Subject Matter Expert for projects and systems.
* Monitor progress, ensure deadlines, and maintain quality.
* Produce reports and performance metrics.
* Drive process improvements and uphold compliance standards.
Requirements:
* 2+ years' relevant office/administration experience.
* Proven people management and leadership skills.
* Strong planning, organisational, and communication abilities.
* Experience handling diverse, high-volume workloads.
* Confidence with workflow/IT systems and performance reporting.
Nice to Have:
* Knowledge of national/EU veterinary regulatory procedures.
* Experience in veterinary medicinal product licensing.
* Project management skills.
Why this role matters
This is a critical position that requires someone who can manage multiple tasks, prioritize effectively, and lead by example. The ideal candidate will have excellent leadership skills, be able to communicate effectively with stakeholders, and have a passion for delivering results.
What you'll get out of it
As a Regulatory Case Manager, you'll have the opportunity to work on challenging projects, develop your skills, and take on additional responsibilities. You'll also have access to training and development opportunities to help you grow in your career.