Location: Chelmsford, UK Department: Operations Directorate Reporting to: Operations Director, UK About the Role We are seeking an experienced Lead (TL) for an 11-month contract to play a pivotal role in establishing and managing a new Chemicals and Materials R&D Unit in Chelmsford, UK. This senior position focuses on delivering consulting services for pharmaceutical and chemical manufacturing facilities, research and development logistics, and outsourced production. As a shared facility, the R&D unit will handle multiple client projects, requiring a hands-on, dynamic leader to drive innovation and operational excellence. The Technology Lead will oversee the design, development, and validation of processes, instruments, and equipment, while also managing clinical information technologies and strategic vendor interactions. This role involves leading cross-functional project teams, ensuring technology solutions align with business objectives, and delivering projects on time, scope, and budget. Key Responsibilities IT Logistics Development: Analyze and optimize business processes to align with technology solutions. Identify and deploy clinical information systems to support product development. Develop and manage project plans, including timelines, resources, risks, and stakeholder communications. Ensure system validation, change control, and stakeholder alignment throughout project lifecycles. Engineering Logistics Setup: Oversee schedules, supplies, equipment, and manpower in the pilot plant, with a focus on solid oral dosage forms. Provide technical leadership in process development, validation, and equipment qualification. Manage technology transfer projects to ensure timely scale-up and product launches. Author and approve technical documentation (SOPs, batch records, validation protocols). Leadership & Collaboration: Lead cross-functional project teams and oversee contractors without direct reports. Foster strong relationships with business leaders, vendors, and stakeholders. Drive operational excellence and innovative solutions in a fast-paced, client-driven environment. Qualifications & Experience MA or PhD in Life Sciences, IT, or Engineering. 10 years of management experience in the biotech or pharmaceutical industry, with expertise in technical development and R&D project implementation. 5 years of professional IT experience in high-performing technical and business environments. Technical expertise in at least one of: parenteral or solid drug product manufacturing/development, biotechnology, chemical production/development, analytical development, or quality control. Strong project management skills (PMP certification a plus). Excellent communication, leadership, and stakeholder management skills. Knowledge of GMP, system validation, and change control processes. Person Specification Proven ability to lead complex projects in a matrix organization, delivering on aggressive milestones. Innovative and forward-thinking, with a focus on scalable, sustainable solutions. Exceptional interpersonal skills to influence and collaborate across functional areas. Hands-on approach with a track record of problem-solving and process optimization.