Senior Quality Director
1 week ago
Senior Quality Director - Pharmaceutical Industry
About Us:We are Dechra, a global specialist in veterinary pharmaceuticals. Our expertise lies in the development, manufacture, marketing, and sales of high-quality products for veterinarians worldwide.
Job Description:As a Senior Quality Director, you will be responsible for managing and leading the Quality teams on site, including Quality Control, Quality Assurance, and Qualified Persons. Your primary focus will be to ensure that quality standards and systems are implemented and maintained in compliance with UK, EU, and FDA cGMP.
Key Responsibilities:- Build positive relationships across site functions to break down existing silos and promote a proactive, solutions-focused culture within the Quality function.
- Deliver results through effective cross-functional collaboration and ensure that the site Quality improvement plan is developed and executed to achieve agreed deliverables, on time, with 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.
- Ensure strategic quality risk management activities are implemented, effective, and sustained by the Quality and site team.
- Coordinate with regulatory authorities, including product recalls, license applications/variation, defect reporting, annual controlled drugs return process, to ensure compliance to current standards.
- Use departmental and site KPIs to monitor and improve performance.
- Ensure the Quality function operates in alignment with the site's 5 strategic pillars (People, Safety, Quality, Deliver & Cost).
- Support the development of the quality team by mentoring and coaching team members, identifying training needs, and implementing a plan to deliver proactively addressing under-performance, developing effective succession plans, and liaising with customers and suppliers as required to resolve any quality issues or deliver further improvements.
- 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 behaviours.
- 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.
- Demonstrated pharmaceutical quality experience, including audit, batch record review, change control, complaint handling, and investigations experience would be beneficial but not needed.
- Knowledge of pharmaceutical/nutraceutical manufacturing, packaging, testing, and distribution processes and associated global regulatory GMP/GDP requirements would be an advantage but not required.
- Experience of hosting UK and FDA inspections, client audits, and self-inspections would be ideal but not required.
- Experience in devising, implementing, and maintaining pharmaceutical quality systems compliance with UK, EU, and FDA GMP requirements would be beneficial but not needed.
- Average 36-hour working week (with a day off every other Friday).
- Plenty of training and development opportunities.
- 22.5 days annual leave + Bank holidays.
- Option to buy a week's holiday each year.
- 8% Employer Pension Contribution.
- Free access to the Headspace App.
- Employee Assistance Programme.
- Free on-site parking.
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The estimated salary range for this position is between $120,000 and $180,000 per annum, depending on qualifications and experience. This estimate is based on industry standards and location factors.
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