Job description summary: Touchlight is focused on developing DNA manufacturing technology for the future of medicine. This technology enables DNA production at unprecedented scale, speed, and purity, and is optimised for use in advanced genetic medicines. Our CDMO and technology are built on the conviction that DNA is fundamental to the future of medicine.
Key activities of the Quality Control Analyst include:
• Environmental monitoring of the GMP facility
• Day-to-day QC testing of raw materials and finished products through molecular biology, microbiology, and biochemistry techniques
• Reagent preparations, goods receipt, sample receipt, procurement, good housekeeping activities, equipment and instrument verifications, and documentation
Requirements of the Quality Control Analyst:
• A degree in a scientific discipline (MSc is a plus)
• Experience working within a GMP environment
• Strong experience of QC environment and organisation, preferably in microbiology
• Proficiency with various QC techniques such as Environmental Monitoring, Bioburden, Gel Electrophoresis, and/or HPLC/UPLC
• Practical experience with aseptic technique
Touchlight is a successful scale-up business with a record of world-leading innovation and a welcoming, entrepreneurial culture. We make Touchlight an extraordinary place to work by providing our employees with incredible facilities, flexible working, and a competitive benefits and remuneration package.