QC Analyst (12 month fixed term contract)

This is what you will do:

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:
• Electrophoresis (SDS-PAGE, IEF, iCE)
• HPLC methods including Size Exclusion, Reverse Phase, Peptide Mapping, Anion Exchange.
• Microplate assays and ELISA
• Protein Concentration
• Compendial Methods such as pH, Osmolality, and Appearance.
• Stability scheduling and testing.
• Provide lab support including reagent preparation, cleaning, and routine equipment maintenance.
• Recognize and report aberrant test results and sample conditions.
• Ensure training is current for all job functions performed.
• Receive and manage samples that come into the lab for stability and release testing.
• Order, stock and receive laboratory supplies.
• Complete all required documentation legibly and accurately.

You will need to have:

• BSc in Chemistry or a biological science, with 1 – 4 years’ experience, or equivalent combination of education and experience.

We would prefer for you to have:

• A working knowledge of the cGMP QC laboratory environment, and equipment associated with testing of biopharmaceutical products
• Ability to follow written procedures with close attention to detail
• Ability to function with minimal supervision for routine job duties. 

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