ReQuire Consultancy are delighted to be supporting a reputable Biosciences organisation based in Salisbury, who are looking to recruit a Senior QC Analyst to join their Quality division.
Working as part of the Development and Manufacturing Group, you will play a key part in being responsible for the provision of analytical chemistry services to support quality control testing of products, raw materials, and water systems.
Main responsibilities include:
Training and supervision of QC staff.
Responsible for writing Standard Operating Procedures and their associated risk assessments to ensure that those tasks are performed safely.
Responsible for writing quality records such as non-conformances, investigations, CAPAs and change controls.
Monitor compliance within QC Analytical, identify weaknesses and develop strategies to continually improve systems.
Verification of QC data.
Have current right to work in the UK.
Ability to work on own initiative, organise own workload and prioritise daily work with minimal supervision working to tight and often changing timescales.
Strong working knowledge / experience of cGMP in a laboratory environment.
Previous experience of standard laboratory equipment and methods.
It is essential that you have experience of the out of specification process and carrying out laboratory investigations.
The post holder will be required to work shift rotation. This includes 2 weeks out of 8 weeks where the shift is 2-10pm, and potential weekend working.
If this role is of interest to you, please contact Carrie for more information or click apply!