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Quality Assurance Specialist
2 months ago
Touchlight is dedicated to "The Making of DNA".
During the Covid pandemic, the significance of our work has been highlighted by the rapid development and scale-up of RNA and DNA-based vaccines. Furthermore, the remarkable advancements in both viral and non-viral cell and gene therapy have intensified the demand for superior quality, expedited, and more reliable DNA manufacturing technologies.
Our Contract Development and Manufacturing Organization (CDMO) is founded on the belief that DNA is essential for the future of healthcare.
By moving beyond conventional biological methods, we have simplified DNA manufacturing. Our proprietary dbDNATM (or "doggybone" DNA) vector is optimized for use in cutting-edge genetic therapies, offering enhanced safety and efficacy compared to traditional plasmid DNA. This platform, based on enzymatic technology, allows for DNA production at unmatched scale, speed, and purity.
We are utilizing our platform to facilitate the next generation of Genetic Medicines.
Our CDMO focuses on:
- Nucleic Acid Medicines (mRNA & DNA)
- Ex-vivo & In-vivo cell and genetic therapies
- Gene therapy utilizing viral vectors and gene editing techniques
- Autologous & Allogenic cell therapies
Quality Control Analyst
Touchlight is in search of a Quality Control Analyst to enhance its Quality Control department. The Quality Control Analyst will play a crucial role in supporting the Quality Control (QC) laboratory with the routine QC testing of manufactured dbDNA for our clients and internal projects.
This position involves close collaboration with other operational teams to address Quality and product requirements. Key responsibilities will encompass the daily QC evaluation of raw and finished products through molecular biology and biochemical methodologies, preparation of reagents, receipt of goods, sample handling, procurement, maintenance of good laboratory practices, verification of equipment and instruments, and thorough documentation.
The QC Analyst will report to the QC Manager and, in support of the Head of Quality Assurance, will ensure compliance with regulatory standards. This role is set in a dynamic, fast-paced environment ideal for self-driven, organized, detail-oriented individuals who can contribute effectively within a diverse and compliance-focused team.
Qualifications:
- A background in a scientific field (MSc is advantageous)
- Experience in a GMP environment, preferably within a CDMO
- Strong background in QC operations and organization
- Experience in reagent preparation and material management
- Proficiency in various QC techniques such as HPLC/UPLC, Bioburden assessment, Environmental Monitoring, and Gel Electrophoresis
Touchlight Benefits:
Touchlight is a thriving scale-up organization recognized for its world-class innovation and a welcoming, entrepreneurial culture. We strive to make Touchlight an exceptional workplace by offering our employees outstanding facilities, flexible working arrangements, and a competitive benefits and compensation package.
A Place for Everyone:
We believe that diversity fosters innovation, and therefore we strongly encourage individuals from all backgrounds to consider opportunities at Touchlight. We are an equal opportunity employer and aim to create a workforce that truly reflects the communities we serve and our customer base.
If you require reasonable adjustments at any stage of the application or interview process, please reach out to our HR team, who will be glad to assist you.
