At Target Healthcare Group, we are committed to revolutionising healthcare. As the UK’s leading manufacturer and supplier of unlicensed medicines and hard-to-source products, we serve retail pharmacies, hospitals, pharmaceutical wholesalers, and homecare markets with unmatched expertise and passion. With a diverse team of over 500 professionals, including pharmacists, skilled technicians, and dedicated support staff, we ensure excellence and innovation in everything we do. Why Top Talent Chooses Us Impact - Ensure the safety and efficacy of life-saving medicines. Innovation - Work with cutting-edge technology and groundbreaking processes in a rapidly growing environment. Career Growth - Enjoy unparalleled opportunities for continuous learning and professional advancement. Collaborative Excellence - Be part of a passionate, international team dedicated to making a real difference in healthcare. Competitive Rewards - Receive a top-tier salary, comprehensive benefits, and enjoy a balanced work-life environment. We're looking to add an Analytical Method Validation Specialist to this busy and fast-paced team. The Role We are looking for an experienced The Analytical Method Validation Specialist to lead the development, validation, transfer, and troubleshooting of analytical methods used in the testing of pharmaceutical raw materials, in-process materials, and finished products. This role ensures all activities comply with regulatory requirements (e.g. EU GMP, ICH) and internal quality standards to support tech transfer and commercial manufacturing. As an Analytical Method Validation Specialist your responsibilities will include, although not limited to: Design and review validation protocols for analytical methods (e.g. HPLC, GC, UV, FTIR, dissolution). Advise on method development, optimisation, and robustness testing in line with ICH guidelines. Ensure proper documentation, including protocols, reports, and lab notebooks meets GMP and regulatory standards. Lead and support method transfer activities between internal departments or external contract labs. Troubleshoot analytical issues and provide technical guidance to QC and manufacturing teams. Collaborate with QA, Regulatory Affairs and Vallidation to support product filings and inspections. Participate in investigations (e.g. OOS, deviations, CAPAs) related to method performance or validation. Maintain and calibrate analytical instrumentation, ensuring proper qualification status (IQ/OQ/PQ). Stay up to date with regulatory expectations and industry best practices for method validation. Support with training in members of the Quality Control department. Collaborate with QA in the auditing of quality control testing laboratories. To be successful in this role, you should be able to demonstrate: Bachelor’s or Masters in Chemistry, Pharmaceutical Sciences or related field. 3-5 years of experience in quality control and technology transfer. Strong knowledge of GMP/GDP and ICH guidelines. Experienced in chromatography and spectroscopic techniques. Excellent analytical and problem-solving skills. Ability to work independently and manage multiple projects Benefits of Working with Us: Joining the Target Healthcare Group means being part of an inspired, enthusiastic team committed to our vision and values. We believe in cultivating a nurturing, dynamic workplace culture. Other benefits include: Active Social and charity committee Cycle to Work Scheme Electric Vehicle Scheme Eye Care Vouchers If you are passionate about quality and aspire to make a significant impact in healthcare, we want you on our team. Join Target Healthcare Group as an Analytical Method Validation Specialist and become a key player in our mission to transform healthcare. Hours of work: Monday – Friday 09.00 – 18.00