We are looking for a skilled and driven Formulation Development Scientist to join our UK manufacturing site. This role acts as the critical technical bridge between our India-based R&D centre and the UK Technology Transfer (TT) department, supporting the seamless transition of liquid products from development through to commercial manufacturing. Key Responsibilities * Lead and support pilot batch manufacturing, scale-up batches, and troubleshooting of commercial batch failures at the UK site. * Serve as the primary technical liaison between the India R&D team and the UK TT department, ensuring effective knowledge transfer and alignment on formulation strategies. * Execute and oversee technology transfer activities for oral liquid and suspension products, ensuring compliance with regulatory requirements and internal quality standards. * Develop and optimize homogenisation processes for large-volume liquid products, ensuring product uniformity, stability, and consistency at scale. * Prepare and review technical documents including batch manufacturing records, technology transfer reports, process descriptions, and deviation investigations. * Identify root causes of manufacturing issues and implement robust corrective and preventive actions (CAPAs). * Collaborate cross-functionally with QA, QC, Regulatory Affairs, and Manufacturing teams to support product lifecycle activities. * Contribute to process validation, equipment qualification, and process analytical technology (PAT) initiatives as applicable. * Stay current with regulatory guidelines (ICH, MHRA, EMA) relevant to liquid dosage form development and manufacturing. Qualifications & Experience Education * M.Pharm / M.Sc. in Pharmaceutics, Pharmaceutical Sciences, or a closely related discipline. * Ph.D. is an advantage but not mandatory. Experience * 6-12 years of hands-on experience in pharmaceutical formulation development, with a focus on oral liquids and suspensions. * Demonstrated experience in scale-up and technology transfer of liquid dosage forms. * Practical experience with homogenisation equipment (high-shear mixers, rotor-stator homogenisers) at pilot and commercial scale. * Prior exposure to a cross-site or cross-functional TT role is highly desirable. Technical Skills * Strong understanding of formulation principles for oral liquids and suspensions (rheology, particle size, physicochemical stability). * Familiarity with ICH Q8/Q9/Q10 guidelines and QbD principles. * Experience with GMP manufacturing environments and documentation practices. * Working knowledge of relevant regulatory frameworks (MHRA, EMA, ANDA/CTD as applicable). Soft Skills * Strong communication skills — able to operate effectively across geographies and functions. * Analytical and structured problem-solving mindset. * Self-driven with the ability to manage multiple priorities independently. * Collaborative team player with a proactive approach