- Nucleic Acid Medicines (mRNA & DNA)
- ex-vivo & in-vivo cell and genetic medicines
- Gene therapy using viral vectors and gene editing
- Autologous & Allogenic cell therapyQuality Control AnalystTouchlight is currently seeking a QC analyst to join its Quality Control department. The Quality Control Analyst is responsible for supporting the Quality Control (QC) laboratory for day-to-day QC testing of manufactured dbDNA for our clients and internal pipeline.
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Quality Control Analyst - Richmond, North Yorkshire, United Kingdom - Touchlight
Description
Touchlight is focussed on" The Making of DNA".Through the Covid pandemic, this quiet revolution has been propelled into the spotlight with the scale-up and proof of concept of RNA and DNA based vaccines.
In addition, the stellar growth in viral and non-viral cell and gene therapy discovery and development has accelerated the need for a better quality, faster and more robust DNA manufacturing technology.
Our CDMO and technology is built on the conviction that DNA is fundamental to the future of medicine. By moving away from today's restrictive biological approaches, we have made DNA manufacturing simple.Our unique dbDNATM (or "doggybone" DNA) vector is optimised for use in advanced genetic medicines, being safer and more efficacious than conventional plasmid DNA.
The platform, based on enzymatic technology, enables DNA production at unprecedented scale, speed and purity.We are leveraging our platform to enable the next generation of Genetic Medicines.
Our CDMO Focus is on:
Key activities will include the day-to-day QC testing of finished product through molecular biology and biochemistry techniques, reagent preparations, goods receipt, sample receipt, procurement, good housekeeping activities, equipment and instrument verifications, and documentation.
The QC Analyst reports to the QC Manager, and in support of the Head of Quality Assurance, to ensure regulatory requirements are met.
This is an exciting, fast-paced environment suited to self-motivated, organised, conscientious and highly accurate individuals, who can contribute to and successfully work in a multi-talented and compliance orientated team.
You have· A background in a scientific discipline (MSc is a plus)· Experience working within a GMP environment, preferably in a CDMO· Strong experience of QC environment and organisation· Experience of reagent preparations and material handlingTouchlight BenefitsTouchlight 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.
A Place for EveryoneWe believe diversity drives innovation and for that reason we strongly encourage those from all backgrounds to apply for roles at Touchlight.
We are an equal opportunity employer and aim to build a workforce that is truly representative of the communities in which we operate and our customers.
If you need reasonable adjustments at any point in the application or interview process, please speak with the HR team who will be happy to support you.
