Meeting all the regulatory standards is vital when you’re developing devices that could have a major impact on people’s lives. Join our Quality Engineering team at our Cambridge site and you’ll play an incredibly important role.

You’ll be involved in everything from ensuring our products deliver the maximum benefits to patients, to monitoring our designs to make sure they meet regulatory requirements. Working closely with Vectura teams around the world, as well as external suppliers, partners and manufacturers, you’ll enjoy a range of experiences, such as addressing patient feedback about products already on the market and taking new products through the manufacturing process.

Join our small pharmaceutical quality team and you’ll enjoy the varied nature of the work we do. This gives you a range of opportunities to learn new skills, work with people across our business and develop into different roles, while still having your own specialist area.

We’ll give you the support you need with training opportunities in everything from quality management systems to specific areas such as cleaning verification. This, in turn, will give you the chance to broaden your experience by tackling new challenges, such as external auditing of our suppliers. In short, you’ll get to see the full picture of our work.

In quality assurance, we ensure that the right processes are in place to help the company operate effectively in every area.

This means you could be involved in a variety of projects, such as overseeing quality management systems and maintaining processes. You could contribute to major infrastructure projects such as buying new equipment or upgrading our IT systems. Or you might be supporting project teams throughout the development cycle for both medical devices and pharmaceutical products.

Contributing to such a wide range of activities and overseeing almost every aspect of what we do, you’ll develop strong working relationships across the whole business.

At Vectura, we recognise that regulatory expertise is vital at every stage of the development process. Our Regulatory and Pharmacovigilance (PV) team are experienced in regulatory development and have submission expertise in the respiratory area (NCEs and generics). They have proven global regulatory success with medical devices and combination products including compliance with MDR as well as global pharmacovigilance and device vigilance capabilities.

Join us and you’ll work with different teams across our business, providing essential regulatory expertise and helping to develop innovative solutions. Working closely with scientists, engineers and a host of other specialists, as well as regulatory bodies around the world, you’ll help to define the regulatory structure for a broad range of products.