Site Quality Director
2 weeks ago
About Dechra
Dechra is a global specialist in veterinary pharmaceuticals, dedicated to developing, manufacturing, marketing, and selling high-quality products exclusively for veterinarians worldwide. Our values of Dedication, Enjoyment, Courage, Honesty, Relationships, and Ambition are deeply embedded in our culture and guide our operations.
The Opportunity
We are seeking a highly motivated and experienced Site Quality Director to lead the quality teams at our Skipton manufacturing facility. This role is crucial in ensuring that our products meet the highest standards of quality and compliance with UK, EU, and FDA cGMP regulations.
Role Responsibilities- Provide strong leadership to the quality team, fostering a culture of excellence and continuous improvement.
- Collaborate effectively with site functions to promote a shared commitment to raising quality standards across all operations.
- Develop and implement a comprehensive quality strategy for the site, encompassing resource allocation, system enhancements, and investment plans.
- Manage departmental activities and resources efficiently, ensuring alignment with budgets, timelines, and established quality standards.
- Drive performance improvements through data analysis, process optimization, and employee engagement initiatives.
- Ensure compliance with all relevant regulatory requirements, including GMP, GDP, and other applicable guidelines.
- Lead internal audits, investigations, and corrective action processes to maintain a robust quality management system.
- Represent the site in interactions with external stakeholders, such as regulatory agencies and customers.
- Extensive knowledge of GMP, UK, EU, and FDA regulations within the pharmaceutical industry.
- Proven experience in quality assurance, audit, batch record review, change control, complaint handling, and investigations.
- In-depth understanding of pharmaceutical manufacturing, packaging, testing, and distribution processes.
- Experience hosting UK and FDA inspections, client audits, and self-inspections.
- Technical expertise to support quality and validation decision-making.
- Strong leadership, communication, and interpersonal skills.
- Degree in Chemistry or a related field, or equivalent experience.
- Eligibility for QP status is highly desirable.
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