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The Executive Director, Quality Assurance Operations leads quality assurance activities in drug substance manufacturing, ensuring compliance with regulations and overseeing a QA team. Responsibilities include managing SOPs, deviation management, training, and maintaining inspection readiness, while ensuring product quality. The role requires extensive experience in biopharmaceutical operations and strong leadership skills.

Provide administrative support for the UK/Northern Cluster team, managing projects, budgets, contracts, travel arrangements, and scheduling meetings while ensuring compliance with legal requirements.

Provide administrative support to Central Cluster in the pharmaceutical industry, manage office operations, and liaise with various teams to ensure compliance and efficiency.

The Associate Director of Marketing in Japan will lead marketing initiatives, manage budgets, build relationships with healthcare professionals, and collaborate with global teams to optimize the launch of medications for rare diseases.

The Head of Biostatistics and Statistical Programming oversees statistical aspects of clinical trials, ensuring integrity and strategic planning in drug development. Responsibilities include leading teams, guiding analysis, mentoring, and collaborating across departments.

The Senior Automation Engineer I designs, implements, and supports Operational Technology networks, leads tech transfers, collaborates for operational improvements, and troubleshoots automated systems in a GMP environment.