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- Tasks: Conduct quality control testing and support laboratory operations for innovative DNA technology.
- Company: Join Touchlight, a pioneer in scalable, cell-free DNA technology transforming genetic medicine.
- Benefits: Enjoy flexible working, competitive pay, and incredible facilities.
- Why this job: Make a real impact in gene therapy while working with cutting-edge technology.
- Qualifications: Degree in a scientific discipline and experience in GMP QC or molecular biology.
- Other info: Diverse and inclusive workplace with excellent career growth opportunities.
The predicted salary is between 36000 - 60000 £ per year.
Touchlight pioneers scalable, cell-free DNA technology, transforming gene therapy and genetic medicine. With a commitment to innovation, excellence, and a diverse team, we push boundaries to deliver safer, more efficient solutions for the future. At Touchlight, we’ve reimagined DNA production to meet the evolving needs of innovators like you. Our patented synthetic DNA vector, dbDNA™, and cell-free enzymatic manufacturing platform deliver DNA with unmatched speed, scale, and purity, helping you move faster from discovery to clinic.
Whether you’re developing mRNA, viral vector, or vaccines, Touchlight helps you overcome the limits of plasmid manufacturing. No cell banking. Just high-quality RUO or GMP DNA, ready when you need it.
Touchlight is currently seeking a Senior Quality Control Analyst to join its Quality Control (QC) department. The Senior QC Analyst is responsible for supporting the Quality Control laboratory for day‑to‑day QC testing of manufactured dbDNA. There will be close interaction with other operational departments to support quality and product needs. Key activities will include day‑to‑day QC testing of raw materials, finished products, and stability samples through molecular biology, biochemistry and microbiology techniques. Testing includes gel electrophoresis, UPLC, Sanger and Nanopore sequencing, endotoxin, and bioburden. Environmental monitoring of GMP cleanroom areas may also form part of the role, depending on operational requirements.
The Senior QC Analyst will also be involved in reagent preparation, goods receipt, sample receipt, procurement, good housekeeping activities, equipment and instrument verification, and documentation. In addition, the Senior QC Analyst will lead and support QMS activities, including laboratory investigations, deviations, CAPAs, risk assessments, and document updates, ensuring investigations are robust, timely, and compliant. As a senior member of the QC function, you will contribute technical expertise, drive high data‑integrity standards, and help the team meet key QC KPIs in a fast‑paced, compliance‑focused environment. The Senior QC Analyst reports to the QC Manager.
Requirements include:
- A degree in a relevant scientific discipline;
- Strong experience working in GMP QC, ideally with molecular biology or nucleic acid testing;
- Experience with raw material testing, stability programmes and nucleic acid product QC;
- Excellent organisational skills, a proactive mindset and high scientific accuracy;
- Ability to thrive in a collaborative, fast‑moving, quality‑driven environment.
We make Touchlight an extraordinary place to work by providing our employees with incredible facilities, flexible working and a competitive benefits and remuneration package. We 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.
Locations
Quality Control Analyst (Permanent) in Cheshire, Hampton employer: Touchlight
Contact Detail:
Touchlight Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Control Analyst (Permanent) in Cheshire, Hampton
✨Tip Number 1
Network like a pro! Reach out to current employees at Touchlight on LinkedIn or other platforms. Ask them about their experiences and any tips they might have for landing a role in the QC department.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of molecular biology and GMP practices. Be ready to discuss how your experience aligns with the day-to-day QC testing and the specific techniques mentioned in the job description.
✨Tip Number 3
Showcase your proactive mindset! During interviews, share examples of how you've taken initiative in past roles, especially in quality control settings. This will demonstrate that you can thrive in a fast-paced, compliance-focused environment.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're genuinely interested in joining the Touchlight team.
We think you need these skills to ace Quality Control Analyst (Permanent) in Cheshire, Hampton
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Senior Quality Control Analyst role. Highlight your GMP QC experience and any relevant molecular biology techniques you've mastered. We want to see how you can contribute to our innovative team!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality control and how your background aligns with Touchlight's mission. Show us your enthusiasm for transforming gene therapy and genetic medicine!
Showcase Your Achievements: Don’t just list your responsibilities; highlight your achievements in previous roles. Did you improve a process or lead a successful project? We love seeing how you’ve made an impact in your past positions, especially in a fast-paced environment like ours.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details about the role and our amazing company culture there!
How to prepare for a job interview at Touchlight
✨Know Your Science
Brush up on your knowledge of molecular biology and nucleic acid testing. Be prepared to discuss specific techniques like gel electrophoresis and UPLC, as well as your experience with GMP QC. This shows you’re not just familiar with the concepts but can apply them in a practical setting.
✨Showcase Your Organisational Skills
Since the role requires excellent organisational skills, think of examples from your past experiences where you successfully managed multiple tasks or projects. Highlight how you prioritised your work and maintained high scientific accuracy under pressure.
✨Emphasise Team Collaboration
Touchlight values a collaborative environment, so be ready to share instances where you worked closely with other departments. Discuss how you contributed to team goals and supported quality and product needs, demonstrating your ability to thrive in a fast-paced setting.
✨Prepare for QMS Discussions
Familiarise yourself with Quality Management Systems (QMS) and be prepared to discuss your experience with laboratory investigations, CAPAs, and risk assessments. Showing that you understand the importance of compliance and data integrity will set you apart as a candidate.