QC Analyst

The individual in this position should have a working knowledge of the cGMP QC laboratory environment and laboratory equipment associated with biopharmaceutical analysis. The position requires the ability to understand and follow written SOPs, to accurately and legibly record work in real time, and pay close attention to detail. The individual must be able to perform routine tasks with a minimum of supervision.

You will be responsible for:

• Perform all lab functions in compliance with cGMP
• Follow written procedures for the following tests, as trained and qualified:
  • Gel electrophoresis (SDS-PAGE, IEF)
  • ELISA and plate based assays (potency and residual assays such as HCP and ProA)
• Prioritisation of samples for testing (release, stability and in-process testing)
• Reviewing of laboratory data, including logbooks and test executions.
• Recognize and report aberrant test results and sampl...