Part of the biologics division of a global pharma organisation this successful company develops and manufactures sterile, bulk products focused on the areas of infection, respiratory and inflammatory disease, oncology and neuroscience, with two marketed products and a robust pipeline of new products. Their UK manufacturing plant is state of the art, employs around 250 and manufactures sterile, bulk vaccines for the treatment of influenza. They supply to export markets being fully FDA and MHRA accredited.
Managing a small team of qualified individuals you will be responsible for the leadership, direction and management of the Quality Assurance Operations department, ensuring that the organisation complies with the relevant cGMPs, policies and standards concerning the manufacturing and control of products. As a leader you will also ensure that corrective action plans are agreed, implemented, monitored and completed. As a QP you will undertake the certification and batch release of product at the site.
The company is embarking on a planned growth phase and investing heavily in new plant and processes which requires the management team to drive and implement change and effective systems across the operation.
You should be a QP (or be working towards your QP qualification) and have QA Operations experience in the vaccine or biologics arena. Ideally you will be working within the biopharma manufacturing sector and be looking to join an ambitious and growing global organisation.
To apply for this position please send your CV to 880098@intersearchuk.com