• Follow QC testing procedures to test parameters and performance of nanoparticles and conjugates in a biomedical service/manufacturing laboratory setting.
• Complete QC records to ensure continued compliance with GxP requirements.
• Manage QC materials and consumables.
• To assist the scientists and lab manager in equipment validation. 
• Utilise a range of methods and techniques for material quality assessment, including pH and UV Vis spectroscopy.
• Work independently to manage release of raw materials and finished goods in a timely manner based on manufacturing timescales.
• Assistance and management of non-conformities including root cause analysis. 
• Working and communicating effectively with other teams.
• Interact with the QA/RA team in order to meet regulatory requirements and ISO 13485 laboratory standard.

• Science based degree, preferably with a high chemistry, biochemistry or biological science content
• Laboratory experience in a regulated environment
• Good numeric and organisational skills and time keeping. 
• Strong attention to detail and accuracy.

Desirable, but not essential:

• Exposure to QC processes
• Knowledge of ISO 13485 or ISO 9001 and GxP.