QUALIFICATIONS

• A BSc in a Life Science subject or other equivalent laboratory experience.

• An exciting opportunity for a Quality Control Analyst I - Analytical to join our team.
• You will support the current GMP production of cellular therapies and cell banking through assay design, development, and validation.
• Perform QC assays and laboratory-based tests including, but not limited to, flow cytometry and endotoxin testing.
• Perform trending, review, and reporting of Quality Control data.
• General record keeping and documentation organisation maintenance.
• Assist in the receipt and release of materials for use within RoslinCT GMP facilities.
• Complete quality related documentation including QC records, change controls, incidents/deviations and risk assessments in accordance to GMP and standard operation procedures.
• Write and update SOPs for QC activities and compile QC reports and certificates of analysis in addition to more general record keeping.
• Participate in day to day running of QC laboratories (perform stock checks, cleaning, waste disposal and coordinating equipment servicing and maintenance).
• Train other members of junior members of staff where necessary (QC Technicians).