At a Glance
- Tasks: Conduct quality control testing and support laboratory operations for innovative DNA technology.
- Company: Join Touchlight, a pioneer in scalable, cell-free DNA technology with a diverse team.
- Benefits: Enjoy flexible working, competitive pay, and incredible facilities in a supportive environment.
- Why this job: Make a real impact in gene therapy and genetic medicine while advancing your career.
- Qualifications: Degree in a scientific discipline; experience in GMP QC and molecular biology preferred.
- Other info: Be part of a fast-paced, collaborative team driving innovation in the biotech industry.
The predicted salary is between 36000 - 60000 ÂŁ 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.
- Involvement in reagent preparation, goods receipt, sample receipt, procurement, good housekeeping activities, equipment and instrument verification, and documentation.
- Leading and supporting 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 employer: Touchlight
Contact Detail:
Touchlight Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Quality Control Analyst
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those at Touchlight. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for the interview by brushing up on your technical skills. Make sure you can talk confidently about molecular biology techniques and QMS processes. We want to see your expertise shine!
✨Tip Number 3
Show us your passion for quality control! Be ready to discuss how you've tackled challenges in previous roles and how you ensure high data integrity. We love candidates who are proactive and detail-oriented.
✨Tip Number 4
Apply through our website! It’s the best way to get noticed. Plus, it shows you're genuinely interested in being part of the Touchlight team. Don’t miss out on this opportunity!
We think you need these skills to ace Senior Quality Control Analyst
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 writing your application, make sure to proofread 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 for the best chance of getting noticed. It’s the easiest way for us to keep track of your application and ensure it reaches the right people. We can’t wait to hear from you!
How to prepare for a job interview at Touchlight
✨Know Your Science
Brush up on your knowledge of molecular biology, biochemistry, and microbiology techniques. Be ready to discuss specific methods like gel electrophoresis and UPLC, as well as your experience with nucleic acid testing. This will show that you’re not just familiar with the theory but can apply it practically.
✨Demonstrate Your Organisational Skills
Since the role requires excellent organisational skills, prepare examples from your past experiences where you successfully managed multiple tasks or projects. Highlight how you maintained high data integrity and compliance in a fast-paced environment, which is crucial for the Senior QC Analyst position.
✨Familiarise Yourself with QMS Processes
Make sure you understand Quality Management Systems (QMS) and good documentation practices. Be prepared to discuss any previous involvement in laboratory investigations, CAPAs, or risk assessments. This will demonstrate your readiness to contribute to the team’s compliance-focused goals.
✨Show Your Collaborative Spirit
Touchlight values teamwork, so think of examples that showcase your ability to work collaboratively in a multi-talented environment. Discuss how you’ve effectively communicated with other departments to support quality and product needs, as this will resonate well with their company culture.