Head of Policy

2 weeks ago


Addlestone, Surrey, United Kingdom Veterinary Medicines Directorate (VMD) Full time

Job Summary:

The Veterinary Medicines Directorate (VMD) is seeking a highly skilled and experienced professional to lead the assessment of the quality requirements of applications for marketing authorisations for biological/immunological veterinary medicinal products (VMPs) in the UK.

Key Responsibilities:

  • Lead and manage the assessors involved in the assessment of safety, efficacy, and overall benefit-risk of biological VMPs.
  • Carry out assessments of certain applications and peer-review those carried out by other team members.
  • Develop and train assessors in areas of safety, efficacy, and quality requirements.
  • Formulate national and international regulatory policies and guidelines for VMPs, including novel therapy VMPs.
  • Provide scientific and regulatory advice to applicants and stakeholders.
  • Lead on VMD's global cooperation initiatives in regulatory affairs, work-sharing across regulatory jurisdictions, and capacity strengthening.

Requirements:

  • Significant experience in regulatory affairs, particularly in the assessment of biological/immunological VMPs.
  • Strong understanding of quality, safety, and efficacy requirements of biological VMPs.
  • Ability to lead and manage a team of assessors.
  • Excellent communication and interpersonal skills.
  • Ability to work effectively in a fast-paced environment.

About the VMD:

The VMD is an Executive Agency of the Department for Environment, Food and Rural Affairs (Defra) and is responsible for ensuring the safety, quality, and efficacy of veterinary medicines in the UK.



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