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Job Description
Job Description
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.
The Role:
- 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 of working in a GMP regulated environment would be beneficial
- Experience of helping manage a QMS and assist with investigations
Please apply online or contact Emma for more information if you feel you have the relevant skill and experience to be considered for this role.