Overview
Are you an experienced QC professional who has worked within a cGMP environment?
SRG have a fantastic opportunity to join a successful and expanding organisation in the Central Belt of Scotland.
Responsibilities
* Development of quality systems, in particular those relating to QC activities of the Quality Department
* Review and approve data such as Environmental Monitoring and QC testing
* Assist with stability study management
* Approve and release incoming Raw Materials
* Management of QMS for QC investigations
* Support analytical method technical transfer and validation
* Carry out a range of analysis such as Environmental Monitoring, endotoxin, bioburden, pH and analytical chemistry based methods
* Support the ongoing maintenance and management of subcontract facilities
* Trending QC data
* Ensure all QC processes are compliant with cGMP guidance
Skills
* Strong communication skills
* Able to work well as part of a team
* Attention to detail
* Time management and planning
Requirements
* Experience in QC release and/or stability testing would be beneficial or experience of similar techniques and lab work
* Experience working with analytical chemistry techniques such as HPLC and/or microbiological methods such as endotoxin and bioburd en testing
* Experience of working in a GMP regulated environment would be beneficial
* Experience of helping manage a QMS and assist with investigations
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