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Interim Quality Director

2 months ago


Skipton, North Yorkshire, United Kingdom Dechra Pharmaceuticals Limited Full time

About Dechra Pharmaceuticals Limited

We are a global specialist in the development, manufacture, marketing, and sales of high-quality products exclusively for veterinarians worldwide.

Our Culture

Our values are embedded within our culture and thrive within our family of almost 2000 colleagues globally. From manufacturing to marketing, Dedication, Enjoyment, Courage, Honesty, Relationships, and Ambition are at the heart of our everyday operations and the way we do business.

The Opportunity

We are seeking an experienced Interim Quality Director to join our team and lead the management and leadership of the Quality teams on site, including Quality Control, Quality Assurance, and Qualified Persons.

Key Responsibilities

  • Lead the Quality function to ensure that quality standards and systems are implemented and maintained in compliance with UK, EU, and FDA cGMP.
  • Develop and execute the site Quality improvement plan to achieve agreed deliverables, on time, with the necessary resources identified, in place, and accountable.
  • Drive performance improvements across departments, recognizing efficiencies while driving continuous quality improvement.
  • Establish and implement visibility of quality on-time performance (OTP) across all departments and drive accountability for resolving quality issues.
  • Coordinate with regulatory Authorities (VMD, FDA, etc.) to ensure compliance to current standards.
  • Monitor and improve performance using departmental and site KPIs.
  • Support the development of the quality team by mentoring, coaching, identifying training needs, and implementing a plan to deliver.
  • Liaise with customers and suppliers as required to resolve any quality issues or deliver further improvements.
  • Host regulatory and customer audits.

Requirements

  • Proven experience in leadership of large functions through line managers and their teams.
  • Strong people management experience.
  • Ability to define and develop a high-performing team culture.
  • Pro-active and solutions-driven with the ability to work to strict deadlines with a high level of accuracy.
  • Role models best practice mindset and behaviors.
  • Ability to prioritize work and handle multiple deadlines.
  • Proven track record of working with multi-department projects.
  • Fully IT literate: Microsoft Outlook, Word, Excel.
  • Knowledge of GMP, UK, EU, and FDA would be beneficial but not required.