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Director of Quality Assurance and Regulatory Compliance
2 months ago
Job Summary:
The Veterinary Medicines Directorate is seeking a highly skilled and experienced professional to fill the role of Head of Quality of Biologicals within our Authorisations Group.
About the Role:
This exciting opportunity will see you at the forefront of animal health and welfare, authorising biological/immunological veterinary medicinal products (VMPs) including vaccines in the UK.
As the Head of Quality of Biologicals, you will be responsible for leading the assessment of the quality requirements of applications for marketing authorisations for biological/immunological VMPs authorised for use in the UK.
Key Responsibilities:
- Lead and manage the assessors involved in the assessment of the quality aspects of biological VMPs and associated work processes.
- Carry out assessments of certain applications and peer review those carried out by other members of the team.
- Develop and train assessors in these areas.
- 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:
To be successful in this role, you will need to have a strong background in quality assurance and regulatory compliance, with experience in leading teams and managing complex projects.
What We Offer:
The Veterinary Medicines Directorate offers a dynamic and supportive work environment, with opportunities for professional development and growth.
How to Apply:
Please submit your application via the Civil Service Jobs website, where you will find a full job description including salary details.
