We are seeking an experienced Interim Quality Director, ideally with QP eligibility to lead the quality department and ensure compliance with all regulatory standards. This role is ideal for a seasoned professional who can provide immediate support, strategic direction, and hands-on leadership to maintain and enhance our quality systems. Key Responsibilities: Oversee all aspects of Quality Assurance and Quality Control, ensuring compliance with GMP, GDP, and other regulatory requirements. Act as the Qualified Person (QP), certifying product release and ensuring safe, compliant product distribution. Lead, mentor, and develop the quality team, fostering a culture of continuous improvement. Drive quality initiatives, corrective actions, and risk management processes to uphold and exceed industry standards. Collaborate cross-functionally to support production, regulatory affairs, and supply chain teams. Qualifications & Experience: Proven experience in Quality Assurance within the pharmaceutical or biotech industry, with QP eligibility. Strong understanding of EU regulatory requirements and GMP guidelines. Demonstrated leadership skills with the ability to influence at all levels. Excellent problem-solving skills and a proactive approach to quality challenges. Contract Details: Location: On-site/Hybrid Duration: 6–12 months, with the potential for extension Start Date: Immediate