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Quality Assurance Specialist

2 months ago

Solihull, Solihull, United Kingdom Touchlight Full time

Touchlight is dedicated to "The Making of DNA".

In light of the Covid pandemic, the significance of DNA and RNA-based vaccines has surged, highlighting the urgent need for enhanced quality and efficiency in DNA manufacturing technologies. The remarkable expansion in cell and gene therapy research has further underscored this necessity.

Our Contract Development and Manufacturing Organization (CDMO) is founded on the belief that DNA is essential for the future of healthcare.

By shifting away from traditional biological methods, we have simplified DNA production. Our proprietary dbDNATM (or "doggybone" DNA) vector is specifically designed for advanced genetic therapies, offering improved safety and efficacy compared to standard plasmid DNA. This platform utilizes enzymatic technology, allowing for DNA synthesis at unmatched scale, speed, and purity.

We are harnessing our technology to support the next wave of Genetic Medicines.

Our CDMO focus encompasses:

  • Nucleic Acid Therapeutics (mRNA & DNA)
  • Ex-vivo & In-vivo cellular and genetic therapies
  • Gene therapy utilizing viral vectors and gene editing techniques
  • Autologous & Allogenic cell therapies

Quality Control Analyst

Touchlight is actively seeking a Quality Control Analyst to become part of our Quality Control division. The role involves supporting the Quality Control (QC) laboratory in the routine QC testing of manufactured dbDNA for both our clients and internal projects.

This position requires close collaboration with various operational teams to address quality and product requirements. Key responsibilities include:

  • Conducting daily QC testing of raw materials and finished products using molecular biology and biochemical techniques
  • Preparing reagents and managing the receipt of goods and samples
  • Overseeing procurement and maintaining good housekeeping practices
  • Verifying equipment and instruments, along with thorough documentation

The QC Analyst will report to the QC Manager and assist the Head of Quality Assurance to ensure compliance with regulatory standards. This dynamic and fast-paced environment is ideal for self-driven, organized, detail-oriented individuals who thrive in a collaborative and compliance-focused team.

Qualifications:

  • A degree in a scientific field (MSc preferred)
  • Experience in a GMP setting, ideally within a CDMO
  • Strong familiarity with QC environments and organizational practices
  • Experience in reagent preparation and material handling
  • Proficiency in various QC methodologies such as HPLC/UPLC, Bioburden testing, Environmental Monitoring, and Gel Electrophoresis

Touchlight Benefits:

Touchlight is a thriving scale-up organization known for its innovative approach and supportive, entrepreneurial culture. We strive to create an exceptional workplace by offering our employees outstanding facilities, flexible working arrangements, and a competitive benefits package.

A Commitment to Diversity:

We believe that diversity fosters innovation, and we strongly encourage individuals from all backgrounds to apply for positions at Touchlight. As an equal opportunity employer, we aim to cultivate a workforce that truly reflects the communities we serve and our clientele.

If you require any accommodations during the application or interview process, please reach out to our HR team for assistance.