Senior Director of Production

Senior Director of Production A clinical-stage biopharmaceutical company developing next-generation Advanced Therapy Medicinal Products (ATMPs) is searching for a new Senior Director of Production. With a growing portfolio of innovative assets in Phase I to III trials, they are establishing a world-class GMP production capability to support thier clinical and future commercial ambitions. Position Overview The Senior Director of Production will lead and manage GMP manufacturing operations for our Phase I–III clinical ATMP programs. This role is critical in ensuring robust, compliant, and timely manufacturing of their therapy products. You will bring strong leadership experience, hands-on knowledge of ATMP production processes, and a solid understanding of the unique challenges of early clinical-stage manufacturing. Key Responsibilities Lead and manage all day-to-day Production operations of the GMP manufacturing facility for clinical ATMP products Oversee Production processes in accordance with EU and FDA GMP regulations Build and manage a multidisciplinary team of Production staff (Managers, Tean Leads, Technicians, Specialists) across Fill/finish operations and Aseptic Processes Develop and maintain production schedules to meet clinical trial supply timelines and regulatory requirements Drive compliance with cGMP in accordance to Germ Drug Law section 12 & 13 and ATMP-specific regulations; ensure readiness for audits and inspections Partner closely with QA, QC, MSAT, Regulatory Affairs, and Process Development to support batch release, deviation management, and process improvements Implement process controls and drive continuous improvement initiatives in a clinical-stage environment Required Qualifications BSc/MSc in Biotechnology, Bioprocess Engineering, Pharmacy, or related life sciences 10 – 15+ years of GMP experience in biopharmaceutical manufacturing, including extensive years at leadership Hands-on experience in clinical-stage ATMP production In-depth knowledge of GMP requirements for clinical trial material (EU/FDA Phase I–III), including aseptic operations and contamination control Proven success leading manufacturing teams and managing multiple concurrent clinical programs Strong organizational, communication, and decision-making skills in a high-paced environment Renumeration Base Salary: €160,000 – €200,000 fixed per annum (depending on experience) Annual Bonus: 10% Long-term Incentives Relocation support If you are interested, click apply or send a direct application to matt.lancaster@discoverinternational.com