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:
1. Development of quality systems, in particular those relating to QC activities of the Quality Department
2. Review and approve data such as Environmental Monitoring and QC testing
3. Assist with stability study management
4. Approve and release incoming Raw Materials
5. Management of QMS for QC investigations
6. Support analytical method technical transfer and validation
7. Carry out a range of analysis such as Environmental Monitoring, endotoxin, bioburden, pH and analytical chemistry based methods
8. Support the ongoing maintenance and management of subcontract facilities
9. Trending QC data
10. Ensure all QC processes are compliant with cGMP guidance
Skills:
11. Strong communication skills
12. Able to work well as part of a team
13. Attention to detail
14. Time management and planning
Requirements:
15. Experience in QC release and/or stability testing would be beneficial or experience of similar techniques and lab work
16. Experience working with analytical chemistry techniques such as HPLC and/or microbiological methods such as endotoxin and bioburden testing
17. Experience of working in a GMP regulated environment would be beneficial
18. Experience of helping manage a QMS and assist with investigations