Production Supervisor, Salisbury

RHL has a long-standing relationship with a leading UK based biopharma manufacturing company, which focuses on unique life-saving vaccination products. Based on ongoing expansion they are recruiting for a Production Supervisor to join their team. Since being established in 2015, the company has doubled in size and is now expanding further. This is one of the few companies which has continued to grow during the Pandemic and has established a strong pipeline of work on which to continue this sustained growth. In this role you will lead the production team and provide production expertise and guidance to the group responsible for the delivery of production activities. You will Implement and utilise a range of production methods and procedures in support of all activities associated with manufacturing. To ensure the facilities are maintained and fit for purpose. Ensure all support activities including Engineering and Validation, required to ensure GMP compliance are scheduled and executed. Supervision and training of staff Responsible for the generation of Non Conformances, CAPAs, Risk Assessments and Change Controls Ensure the unit is ready at all times for audit by any regulatory organisation Responsible for the provision of all consumables and, supplies required for day to day activity. Identify, evaluate and adapt new technologies where appropriate and ensure that the production area operates to a high standard and complies with GMP and other regulatory standards. Provide reports on all aspects of manufacturing as requested. They are looking for? Someone with a degree in a biological sciences or relevant discipline, or significant relevant experience. Experience working in a clean room environment including a management/supervisory role in GMP manufacturing environment Writing and reviewing batch documentation and SOPs Downstream processing experience Batch and facility planning to support schedules including monitoring, adjusting and ensuring compliance with schedules Experience of managing teams of technical staff Comprehensive understanding of critical utilities, calibration, Validation, and maintenance activity associated with a GMP environment If you feel you are a good fit for this role please apply below