Site Director (GMP)

• Provide overall leadership for site operations, ensuring safety, quality, delivery, and cost KPIs are met.
• Develop and execute the site’s operational strategy in alignment with corporate objectives.
• Oversee end-to-end supply-chain activities, including production scheduling, inventory management, and on-time delivery.
• Champion GMP compliance and maintain inspection readiness with global regulators (FDA, EMA, MHRA, etc.).
• Lead continuous improvement initiatives and drive capital projects and technology upgrades.
• Own site-level budgeting and financial performance, including variance analysis and corrective actions.
• Build and mentor a high-performing team, fostering a culture of accountability and collaboration.
• Act as the key liaison between site operations, corporate functions, and external stakeholders.

Required Skills & Experience

• 10–15 years of experience in GMP-regulated manufacturing, with 5+ years in senior site leadership.
• Strong track record managing cross-functional operations in a matrixed environment.
• In-depth knowledge of GMP, quality systems, and regulatory compliance (FDA, EMA, MHRA).
• Demonstrated experience with site P&L, capital projects, and operational strategy.
• Excellent leadership, communication, and stakeholder management skills.
• Proficiency in enterprise systems (e.g., SAP, Oracle) and modern manufacturing technologies.
• Degree in Engineering, Chemistry, Pharmacy, or related discipline; advanced degree preferred.