GxP Recruitment invites applications on behalf of our biopharmaceutical client in Grangemouth where an excellent new opportunity has arisen for a Senior QC Analytical Chemist to join their team on a permanent basis.
This is a Monday to Friday role based on 37.5 hours with flexitime.
Job Purpose:
The Senior QC Analytical Chemist will supervise and carry out defined QC testing for the release of raw materials, intermediates, bulk drug substances and final products.
Key duties include:
Apply best cGMP work-practices and techniques to test and release raw materials, in process products, bulk drug substance, final products and stability products within specification
Ensure that all QC analysts are appropriately trained and competent in the procedures they are conducting, and are in compliance with best cGMP working practices at all times.
Conduct on-time reporting
review and verification of analytical data provided by the QC Analysts
Immediately escalate and report any deviations to materials, facilities, processes or procedures to the QC Manager
Be accountable for the analytical laboratories being clean, tidy and well organized and in a state of continuous inspection readiness.
Issue, manage and close-out deviations, change controls, OOS or SST investigations and CAPA s in a timely fashion
Identify areas for continuous improvement and escalate those to the QC Manager.
Support the transfer of new methods and techniques into Quality Control.
The ideal candidate:
Min. 4 years experience in a GMP laboratory environment
Some supervisory experience
HPLC experience
Experience of writing deviations and investigating OOS