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An established industry player is seeking a Head of Technical Transfer to oversee GMP and non-GMP manufacturing operations. This pivotal role involves ensuring compliance with regulatory standards, leading a talented team, and facilitating the development of processes for technical transfer. The company is committed to innovation and quality, providing tailored solutions to accelerate drug development. With a focus on team performance and stakeholder engagement, this position offers a unique opportunity to make a significant impact in a rapidly expanding environment. If you are a results-oriented leader with a technical mindset, this is the perfect chance to advance your career.
Upperton Pharma Solutions is a leading Nottingham-based contract development and manufacturing organisation (CDMO) specialising in formulation development, clinical trial manufacturing and manufacturing services for a wide range of dosage forms, including oral solids, liquids, semi-solids, and inhalation products.
With state-of-the-art facilities and a team of experienced scientists, Upperton offers tailored solutions to accelerate drug development from concept to commercialisation. Upperton is committed to innovation, quality, and shares in our customers' dedication to changing the lives of patients.
Upperton collaborates closely with global pharmaceutical and biotech companies to bring novel therapies to market efficiently and effectively.
Continued growth and investment into the business has led to the creation of exciting new job opportunities in our new GMP Manufacturing headquarters in Beeston, Nottingham. Upperton Pharma Solutions is undergoing a period of significant expansion to meet international customer demand and offer a comprehensive drug development portfolio, so now is a great time to join our team.
The Head of Technical Transfer is responsible for all GMP and Non-GMP manufacturing operations, including but not limited to process development, scale up, technical batch manufacture and technical transfer activities. The post holder's responsibilities will also include operational activities within the Unit 3 manufacturing facility and equipment for which these operations are conducted. The role will have direct line management responsibility for operational staff within these functional areas. The post holder will ensure that all operations are developed and conducted within the framework of the Upperton Pharma Solutions Quality Management System and that the facility and operation are qualified to meet the regulatory requirements as set out by regulatory authorities. The post holder will also be responsible for building operational capabilities for commercial manufacturing.
Main Duties And Responsibilities