Are you an experienced QC professional who has worked within a cGMP microbiology 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
- Carry out a range of microbiological testing
- 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:
- Knowledge of and experience in regulated industrial microbiology/cleanroom environments
- Experience of working in a GMP regulated environment would be beneficial
- Experience of helping manage a QMS and assist with investigations
Experience of some or all of the below is essential:
- Plate enumeration
- Subculture
- Growth promotion (solid and liquid media)
- Gram stain
- Morphology
- Bioburden validation
- Sterility validation
- Endotoxin validation and test by kinetic methods (turbidimetric and chromogenic)
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.