• Prepare glassware and reagents used in the manufacturer of buffers and liquid conjugates.
• Manage storage of the reagents, buffers and conjugates.
• Packing and handling of finished materials.
• Follow defined standard operating procedures (SOPs), initially under supervision, but quickly transitioning to independent working, in a biomedical
  service/manufacturing laboratory setting.
• To be compliant with GxP systems and procedures covering this facility, including the completion of manufacturing batch records.
• Utilise a range of methods, assays techniques in assay manufacturing.
• Working and communicating effectively with team members.
• Interact with the QA/RA team in order to meet regulatory requirements and ISO 13485 laboratory standard.

• A-level with good marks in maths, chemistry and biology.
• Good numeric and organisational skills and time keeping. Strong attention to detail and a high level of organisation.
• Strong interpersonal and communication skills in particular, reporting information in a clear and systematic fashion. Good teamwork and ability to communicate clearly and follow instructions.
• Pro-active attitude and strong interest in molecular diagnostics (QC and/or manufacturing).

Desirable, but not essential:

• BSc in Analytical chemistry, Chemical Engineering, Process chemistry, Biochemistry, Industrial Biotechnology or equivalent.
• Knowledge of ISO 13485 or ISO 9001 and GxP.