Our client develops innovative solutions for effective cancer treatments to improve patients' lives. The needs of patients are at the centre of their work, ensuring they provide affordable, accessible medicines that have a real impact.ResponsibilitiesManage and oversee new product introduction and technology transfer, and support registrations.Liaise with other internal departments to ensure all necessary systems are implemented in a timely manner and in line with project plans.Prepare, review, and approve relevant Standard Operating Procedures (SOPs) and other necessary GMP and GDP documents.Conduct and support manufacturing process investigations to facilitate operational excellence and continuous improvement.Identify continuous improvement and implementation of process improvement and operational excellence projects and liaise with key stakeholders and external vendors to support these projects.Drive the team (internal and external) towards operational excellence, optimizing manufacturing processes and ensuring product quality.Monitor manufacturing process compliance issues.Manage events as required ensuring appropriate communication within the team and external team.Qualifications10 years’ relevant experience in a cGMP pharmaceutical manufacturing environment.BSc in a science related discipline (Chemistry, Engineering, Biotechnology etc).Experience working with multiple dosage forms of drug products and in multiple manufacturing process areas such as tech transfer, process validation, process optimisation, and routine manufacture.Seniority levelMid-Senior levelEmployment typeFull-timeJob functionEngineering and ManufacturingIndustriesPharmaceutical Manufacturing
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