Lonza is a world leader in cell & gene therapy manufacturing, working across a variety of modalities. In this fast-paced and high-growth environment, we are always looking to hire new talent across our network. Open positions include roles in QA/QC, Process Development, Assay Development, Manufacturing Science and Technologies (MSAT), Regulatory Affairs and Operations.

Senior Manager, Quality Operations (Cell Therapy)

The Sr. Manager, Quality Operations leads a team of QA OTF Specialists and QA Project Managers responsible for supporting Lonza's internal and external customers. The manager ensures staff is meeting objectives and deliverables on time and in full, and plays a key role within the site leadership team. This position supports the overflow of tasks as needed, assigns resources and priorities, ensures adequate training, coaches and develops staff, and evaluates performance.

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Quality Sterility Assurance Manager

In this role you will be responsible for quality assurance oversight of Aseptic Processing Program, Environmental Monitoring and Microbial Control Policies for the Cell Therapy and/or Viral Therapy Operations. Your primary responsibility is to maintain sterility assurance of Aseptically manufactured sterile drug products and viral vector products. You need to be able to work independently with little direction to review policies and procedures and related completed media fill/APS documentation, Environmental Monitoring sample plans, cleanroom qualifications, environmental monitoring excursions, deviations and sterility failures.

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A career at Lonza in Cell & Gene Technologies (CGT) offers you exposure to various pharmaceutical players, to the next big blockbuster product of tomorrow and provides you with the necessary skill-set to understand and meet both our – and our customers’ – expectations. By joining Lonza, you’ll get to work with some of the world’s top experts in the space, while developing advanced therapies with a potentially life-saving outcome.

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