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The Scientist will support the development and optimization of automated manufacturing processes for cellular therapies, design experiments, author technical documents, and ensure GMP compliance. The role involves collaborating with teams and conducting analytical assays to support process development.

The Senior Scientist in Process Development will focus on the development and support of autologous and allogeneic cellular therapy products, particularly allogeneic CAR NK therapies. Responsibilities include leading process development experiments, validating manufacturing processes, coordinating technical documentation, supporting GMP manufacturing, and collaborating with various departments to ensure successful technology transfers and compliance with industry standards.

The Data Engineer/Architect will design, build, and maintain data infrastructure and pipelines. Responsibilities include optimizing ETL processes, managing data warehouses and lakehouses, utilizing Azure and Snowflake, and collaborating with stakeholders to deliver data solutions.

The Global Operations Project Manager will oversee the execution of major corporate projects, focusing on operational excellence and efficiency improvements. This includes managing integrated project plans, monitoring project metrics, and ensuring alignment with organizational goals. The role involves collaboration with executive leadership and cross-functional teams to achieve project objectives on time and within budget.

Seeking a motivated and proactive HR Generalist to partner with HR Business Partners and enhance HR support for a growing manufacturing site. Responsible for various HR programs, including talent acquisition, talent management, performance management, and employee engagement. Provides support in areas of workforce planning, employee relations, HR policies, compliance, and talent management programs.

The Operations Support Specialist at Legend Biotech in Raritan, NJ, is responsible for supporting process operations in a sterile cGMP environment. Key responsibilities include performing support tasks, maintaining data records, building strong partnerships, and driving continuous improvements in cell therapy Technical Operations. The role requires a high school diploma with relevant experience, proficiency in computer skills, ability to work independently, and knowledge of cGMP regulations and FDA guidance.

The Operations Associate at Legend Biotech in Raritan, NJ, is responsible for manufacturing procedures in a CGMP environment, ensuring quality standards and compliance with regulations. Key responsibilities include executing manufacturing processes, maintaining documentation, supporting production tasks, and driving continuous improvement.