Are you looking for a rewarding career in healthcare manufacturing? Join Target Healthcare Group, a pioneering pharmaceutical developer and manufacturer dedicated to innovation and saving lives. As part of our Group, Quantum Pharmaceutical is the UK’s leading manufacturer and supplier of unlicensed medicines and hard-to-source products. With over 500 professionals across various disciplines—including pharmacists, technicians, IT, HR, procurement, warehouse, and customer service—we are one of the fastest-growing healthcare companies in the UK. We are currently seeking a passionate Head of Operational Quality and Formulation to join our Aseptic Services team, a key part of our operations, where we manufacture life-saving chemotherapy drugs. Why This Role Matters This isn’t just a job—it’s an opportunity to make a real difference. You’ll be part of a team that values growth, innovation, and professional development. Your Responsibilities Product Release Overseeing processes, policies and quality teams to ensure timely and safe release of manufactured products in compliance with GMP, internal SOPs and regulatory standards. Act as Quality Controller on the Manufacturers Specials License for the Burnopfield manufacturing site in line with MHRA requirements. Establish, monitor and report on key quality related release metrics including: Batch release timelines and adherence to SLA. Right-First-Time (RFT) release rates. Turnaround time for resolution of batch release issues. Lead monthly performance reviews and contribute to site-level Quality Manager Review (QMR) forums. Identify bottlenecks and lead initiatives to streamline batch documentation, review workflows and reduce release cycle time. Implement and track continuous improvement projects using structured methodologies. Collaborate with Production, Warehouse, training and QA to improve coordination and reduce repeat errors. Formulation and Product Introduction Manage and guide new product introduction from technical feasibility to production readiness. Liaise with production and procurement teams to assess and control new starting materials and formulations. Act as a Superuser for the electronic manufacturing system to ensure formulations are developed and manufactured according to GMP, internal SOPs and regulatory standards. Stability and Lifecycle Design and oversee stability programs in alignment with regulatory requirements. Own and monitor product lifecycle data. Lead root cause investigations and implement CAPAs related to formulation and product performance. Ensure pharmacovigilance systems are in place and monitor adherence. Quality Systems and Compliance Lead deviation investigations, customer complaint assessments, risk assessments and change controls as required. Maintain and update SOPs, protocols and technical documentation. Ensure compliance with GMP, GDP and MHRA Regulations Support audits and contribute to PQRs, product recalls and QMS reviews. What We’re Looking For GPhC registration is essential. Minimum 5 years' experience in pharmaceutical formulation, QA, or manufacturing. Strong knowledge of GMP, GDP, and MHRA Specials guidance. Excellent communication, leadership, and project coordination skills. Strong data analysis and process improvement mindset. Comfortable working in fast-paced, regulated, multi-site environments. Experience of operating in a similar role is desirable. Why Join Us? Career Growth - Elevate your expertise in a fast-growing, cutting-edge industry Flexible Shifts – Between our 24-hour core operating hours, Monday – Sunday Pension & Benefits – Including a cycle-to-work scheme Free Food & Drinks – Enjoy complimentary refreshments at work Vibrant Work Culture – A strong Social Committee organises regular events