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QA Batch Release Associate聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽聽
Liverpool
Up to 拢19.44 per hour
6 months contract
CPL Life Sciences are currently partnering with a large biotechnology development company to support a 6-month contract hire in the Liverpool area. The responsibilities of the role will include working across the quality department to compile and review batch documentation and data for release, ensuring adherence to cGMP requirements and escalate possible issues.
MAIN DUTIES AND RESPONSIBILITIES
路聽聽聽聽聽聽聽Previous experience in a similar role within the pharmaceutical industry and knowledge of cGMP requirements.
路聽聽聽聽聽聽聽Experience with quality assurance, and knowledge of quality management systems (i.e., Trackwise, Veeva, and SAP) are preferable.
路聽聽聽聽聽聽聽Completion and timely closure of PTC and deviation investigations, identifying and escalating potential trends, performing thorough investigations, and implementing appropriate CAPAs.
路聽聽聽聽聽聽聽Ensuring timely completion of root cause investigations and escalating critical items to management.
路聽聽聽聽聽聽聽Demonstrated communication skills (written and verbal), and ability to work independently and within a team environment.
路聽聽聽聽聽聽聽Working cross-functionally, providing support and oversight across different functions to instill and promote a quality culture.
For further information please apply within or send your CV to
