Walker Cole International is seeking a dynamic Head of Formulation to join a growing pharmaceutical CDMO in the South of England. This is an exciting opportunity for an experienced leader in formulation development, with a focus on driving the successful development and commercialization of oral solid dosage forms, while overseeing project management, team leadership, and innovation in pharmaceutical drug product manufacturing. Key Responsibilities: Formulation Development: Design, plan, and develop robust formulations from concept to commercial launch, ensuring required claims, novel technologies, excipient/packaging compatibility, product performance, physical characteristics, physicochemical stability, sustainability, risks, and costs are considered. Project Management: Manage multiple projects simultaneously, ensuring methodical experimental design, meticulous execution, and precise data analysis, guaranteeing timely milestone completion and smooth transition from development to commercialization. Team Leadership and Mentorship: Lead and mentor a small team of Formulation Chemists, providing direction, training, and development opportunities, ensuring team members grow their skills and maintain training records. Collaboration & Stakeholder Communication: Act as the main point of contact for development projects, liaising with clients, internal teams, and stakeholders to ensure effective communication and smooth project execution. Process Innovation and Optimization: Drive innovation in formulation techniques and continuously seek improvements to enhance product quality, efficiency, and sustainability. GMP Compliance & Regulatory Adherence: Ensure all formulations meet the highest GMP compliance and regulatory requirements, applying Quality by Design (QbD) principles throughout the development processes. Documentation and Reporting: Document all R&D activities accurately and in a timely manner, ensuring that batch records, stability reports, development protocols, and other necessary documents meet regulatory standards. Product and Technology Transfer: Collaborate with cross-functional teams to manage the seamless transfer of new formulations from development to production and commercialization. Required Experience and Skills: A degree in Pharmaceutical Sciences, Chemistry, or a related field. Several years of experience in formulation development, particularly with oral solid dosage (OSD) forms, and a solid background in pharmaceutical CDMO environments. Proven experience in leading formulation projects from concept through to commercial launch, focusing on novel technologies and excipient/packaging compatibility. Strong project management skills, with the ability to manage multiple concurrent projects while maintaining high standards of execution. Leadership experience with the ability to manage and mentor a small team of scientists, ensuring the development of their skills and expertise. In-depth knowledge of GMP standards and regulatory compliance in pharmaceutical formulation development. Expertise in drug product manufacturing techniques, such as granulation, compression, coating, and other key OSD manufacturing processes. Excellent communication and organizational skills, with the ability to collaborate effectively across teams and engage with clients and stakeholders. Formulation | Pharmaceutical | CDMO | OSD | GMP | Quality by Design | Drug Product Manufacturing Techniques | Oral Solid Dosage | Project Management | Team Leadership | Regulatory Compliance | Product Development | Technology Transfer | Granulation | Compression | Coating | Pharmaceutical Sciences