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- Tasks: Join our QC team to ensure top-notch testing of innovative DNA products.
- Company: Touchlight is revolutionising DNA manufacturing for the future of medicine.
- Benefits: Enjoy flexible working, competitive pay, and amazing facilities.
- Why this job: Be part of a groundbreaking company making a real impact in genetic medicine.
- Qualifications: A degree in a scientific field is essential; experience in QC is a plus.
- Other info: We celebrate diversity and encourage applicants from all backgrounds.
The predicted salary is between 36000 - 60000 £ per year.
Through the Covid pandemic, this quiet revolution has been propelled into the spotlight with the scale-up and proof of concept of RNA and DNA based vaccines. In addition, the stellar growth in viral and non-viral cell and gene therapy discovery and development has accelerated the need for a better quality, faster and more robust DNA manufacturing technology. Our CDMO and technology is built on the conviction that DNA is fundamental to the future of medicine. By moving away from today's restrictive biological approaches, we have made DNA manufacturing simple. Our unique dbDNAâ„¢ (or "doggybone" DNA) vector is optimised for use in advanced genetic medicines, being safer and more efficacious than conventional plasmid DNA. The platform, based on enzymatic technology, enables DNA production at unprecedented scale, speed and purity. We are leveraging our platform to enable the next generation of Genetic Medicines.
- Nucleic Acid Medicines (mRNA & DNA)
- Ex-vivo & in-vivo cell and genetic medicines
- Gene therapy using viral vectors and gene editing
- Autologous & Allogenic cell therapy
Touchlight is currently seeking a QC analyst to join its Quality Control department. The Quality Control Analyst is responsible for supporting the Quality Control (QC) laboratory for day-to-day QC testing of manufactured dbDNA and environmental monitoring activities. There will be a close interaction with the other operational departments to support Quality and product needs. Key activities will include environmental monitoring of the GMP facility and the day-to-day QC testing of raw materials and finished products through molecular biology, microbiology and biochemistry techniques. Testing includes bioburden, endotoxin, gel electrophoresis, pH, and HPLC/UPLC. The QC analyst will also be involved with reagent preparations, goods receipt, sample receipt, procurement, good housekeeping activities, equipment and instrument verifications, and documentation. The QC Analyst reports to the QC Manager, and in support of the Head of Quality Assurance, to ensure regulatory requirements are met.
A degree in a scientific discipline (MSc is a plus). Strong experience of QC environment and organisation, preferably in microbiology. Proficiency with various QC techniques such as Environmental Monitoring, Bioburden, Gel Electrophoresis, and/or HPLC/UPLC.
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.
Pharmaceutical Quality Control Analyst employer: Touchlight
Contact Detail:
Touchlight Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmaceutical Quality Control Analyst
✨Tip Number 1
Familiarise yourself with the specific QC techniques mentioned in the job description, such as bioburden testing and HPLC/UPLC. Being able to discuss these methods confidently during your interview will show that you have the relevant knowledge and skills.
✨Tip Number 2
Network with professionals in the pharmaceutical quality control field. Attend industry events or join online forums where you can connect with current employees at Touchlight or similar companies. This can provide you with insider insights and potentially a referral.
✨Tip Number 3
Research Touchlight’s unique dbDNA™ technology and its applications in genetic medicine. Understanding the company's mission and how your role as a QC Analyst fits into their goals will help you articulate your enthusiasm and alignment with their vision during the interview.
✨Tip Number 4
Prepare to discuss your experience in a QC environment, particularly in microbiology. Be ready to provide examples of how you've contributed to maintaining quality standards and compliance in previous roles, as this will demonstrate your capability to meet regulatory requirements.
We think you need these skills to ace Pharmaceutical Quality Control Analyst
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality control, particularly in microbiology and the specific techniques mentioned in the job description, such as HPLC/UPLC and gel electrophoresis.
Craft a Compelling Cover Letter: In your cover letter, express your passion for the pharmaceutical industry and how your background aligns with Touchlight's mission. Mention any specific experiences that demonstrate your proficiency in QC techniques.
Highlight Relevant Skills: Clearly outline your skills related to environmental monitoring, bioburden testing, and documentation practices. Use specific examples from your past roles to illustrate your expertise.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in a QC role.
How to prepare for a job interview at Touchlight
✨Know Your Techniques
Familiarise yourself with the specific QC techniques mentioned in the job description, such as bioburden testing, gel electrophoresis, and HPLC/UPLC. Be prepared to discuss your experience with these methods and how you've applied them in previous roles.
✨Understand the Company’s Mission
Research Touchlight's unique dbDNAâ„¢ technology and its significance in the field of genetic medicines. Showing that you understand their mission and how your role contributes to it can set you apart from other candidates.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills in a QC environment. Prepare examples of how you've handled challenges in past roles, particularly those related to quality control and regulatory compliance.
✨Highlight Team Collaboration
Since the role involves close interaction with other operational departments, be ready to discuss your teamwork experiences. Share examples of how you've successfully collaborated with colleagues to achieve quality and product needs.
