Preferred Qualifications: Project management and prioritization skills gained within a complex matrix Excellent problem solver and ability to think and work creatively Strong technical acumen and communication skills with the ability to articulate complex, technical details to stakeholders and enable cross functional collaboration across sites, supply chain, R&D and suppliers Experience managing external partners/CDMO's in NPI and/or commercial supply Ability to effectively influence stakeholders at all levels Work Location: This role can be based in Ware, Worthing, Barnard Castle, UK or Upper Merion or Durham, USA and offers a hybrid working model, combining on-site and remote work. Qualifications/Skills Basic Qualifications: University Degree (minimum) in Chemistry, Chemical engineering, Pharmaceutical Sciences or similar area Extensive years' experience in pharmaceutical development and/or manufacturing, ideally in small molecule modality Comprehensive knowledge of external regulatory requirements (MHRA, FDA), and internal/external quality and safety requirements Experienced in technology transfer, with an understanding of the product development process Knowledge of current and emerging Regulatory Strategies (Quality by Design, GMP for 21st century, ICH Q7, Q8, Q9, Q10) and Product Lifecycle Management Demonstrated experience in the pharmaceutical industry in leading the technical aspects of Product Lifecycle Management, including supporting process investigations.