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For Companies At a Glance
- Tasks: Conduct quality control testing and support laboratory operations in a fast-paced environment.
- Company: Join Touchlight, a pioneer in cell-free DNA technology and innovation.
- Benefits: Enjoy flexible working, competitive pay, and a vibrant workplace culture.
- Other info: Diverse and inclusive team with excellent career growth opportunities.
- Why this job: Make a real impact in gene therapy and genetic medicine with cutting-edge technology.
- Qualifications: Degree in a scientific field; experience in GMP QC and molecular biology preferred.
The predicted salary is between 36000 - 60000 £ per year.
About Us
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 fermentation. No antibiotics. No cell banking. Just high-quality RUO or GMP DNA, ready when you need it.
Role Overview
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.
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.
Skills and Experience
- A degree in a relevant scientific discipline; MSc beneficial
- 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
- Practical knowledge of QMS processes and good documentation practices
- Excellent organisational skills, a proactive mindset and high scientific accuracy
- Ability to thrive in a collaborative, fast-moving, quality-driven environment.
Touchlight Benefits
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.
A Place for Everyone
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. 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.
Senior Quality Control Analyst in Hampton employer: Touchlight
Contact Detail:
Touchlight Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Quality Control Analyst in Hampton
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand their mission and values, especially how they relate to quality control in gene therapy. This will help you tailor your answers and show you're genuinely interested.
✨Tip Number 3
Practice common interview questions, but also be ready for technical ones related to QC processes and molecular biology techniques. We recommend doing mock interviews with friends or mentors to build confidence.
✨Tip Number 4
Apply through our website for the best chance of getting noticed. Make sure your CV highlights relevant experience and skills that match the Senior Quality Control Analyst role. We want to see what makes you stand out!
We think you need these skills to ace Senior Quality Control Analyst in 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 our mission at Touchlight. Let us know what excites you about working in a fast-paced, compliance-focused environment.
Showcase Your Attention to Detail: In the world of quality control, accuracy is key. When filling out your application, double-check for any typos or errors. We appreciate candidates who demonstrate high scientific accuracy and attention to detail right from the start!
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 info you need about the role and our amazing company culture!
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 processes. This will show that you’re not just familiar with the theory but can apply it practically.
✨Showcase Your Organisational Skills
Since the role requires excellent organisational skills, come ready with examples of how you've managed multiple tasks or projects in a fast-paced environment. Highlight any experiences where your proactive mindset led to successful outcomes, especially in quality-driven settings.
✨Understand QMS Processes
Familiarise yourself with Quality Management Systems (QMS) and good documentation practices. Be ready to discuss how you've contributed to laboratory investigations, CAPAs, or risk assessments in previous roles. This will demonstrate your ability to maintain high data integrity standards.
✨Emphasise Team Collaboration
Touchlight values teamwork, so be prepared to share examples of how you've successfully collaborated with others in a multi-talented environment. Discuss how you’ve supported colleagues in achieving key QC KPIs and how you handle challenges within a team setting.