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- Tasks: Join us as a QC Microbiology Analyst, performing microbiological testing and environmental monitoring.
- Company: Touchlight is revolutionising genetic medicines with innovative DNA manufacturing technology.
- Benefits: Enjoy flexible working, competitive pay, and amazing facilities in a supportive environment.
- Why this job: Be part of a collaborative team making a real impact in the future of medicine.
- Qualifications: A degree in a scientific discipline and at least 1 year of QC microbiology experience required.
- Other info: We celebrate diversity and encourage applicants from all backgrounds to apply.
The predicted salary is between 30000 - 42000 £ per year.
About Us
Do you want to work with a team that is changing science and enabling the next generation of genetic medicines? The stellar growth in cell and gene therapy has accelerated the need for a better quality, faster and more robust DNA manufacturing technology. Touchlight has created a new DNA vector for use in advanced genetic medicines that is safer and more efficacious than conventional plasmid DNA. Our unique platform also enables DNA production at unprecedented scale, speed and purity. We believe that DNA is fundamental to the future of medicine and our CDMO has a focus on the following areas:
- Nucleic acid medicines (mRNA and DNA)
- Ex-vivo and in-vivo cell and genetic medicines
- Gene therapy using viral vectors and gene editing
- Autologous and allogenic cell therapy
Role Overview
Touchlight is currently seeking a QC Microbiology Analyst to join its Quality Control department. This role is responsible for performing microbiological testing of manufactured dbDNA and environmental monitoring activities of the classified GMP facilities. Key activities will include environmental monitoring, QC testing of finished product by bioburden and endotoxin methods, microbiological identification, and general lab housekeeping and maintenance activities. The role will include development opportunities working with the QC Analytical team on finished product testing being trained on methods, including gel electrophoresis, UPLC, and spectrophotometry. This is an exciting, collaborative 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 scientific discipline
- Experience working within a GMP environment
- Minimum 1 year experience in a QC microbiology laboratory
- Practical experience with aseptic technique
- Proficient at environmental monitoring of classified cleanrooms
- Experience with QC microbiological techniques; bioburden and endotoxin testing
- Competent in document completion to GMP principles
- Detail oriented and organised.
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.
Quality Control Microbiology Analyst employer: Touchlight
Contact Detail:
Touchlight Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Control Microbiology Analyst
✨Tip Number 1
Familiarise yourself with the latest microbiological testing techniques, especially bioburden and endotoxin methods. Being able to discuss these methods confidently during your interview will show that you're proactive and knowledgeable about the role.
✨Tip Number 2
Highlight any experience you have in a GMP environment. Be prepared to share specific examples of how you've maintained compliance and contributed to quality control processes in previous roles.
✨Tip Number 3
Demonstrate your understanding of aseptic techniques and environmental monitoring. You could even mention any relevant training or certifications you have that relate to these areas, as this will set you apart from other candidates.
✨Tip Number 4
Show your enthusiasm for working in a collaborative and innovative environment. Research Touchlight's recent advancements in DNA manufacturing and be ready to discuss how you can contribute to their mission during your interview.
We think you need these skills to ace Quality Control Microbiology Analyst
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and required skills for the Quality Control Microbiology Analyst position. Tailor your application to highlight how your experience aligns with these requirements.
Highlight Relevant Experience: Emphasise your experience in a GMP environment and any specific microbiological techniques you have used, such as bioburden and endotoxin testing. Use concrete examples to demonstrate your proficiency and attention to detail.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for the role and the company. Mention why you are interested in working at Touchlight and how you can contribute to their mission in genetic medicines.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role in quality control.
How to prepare for a job interview at Touchlight
✨Know Your Microbiology Basics
Brush up on your microbiological testing methods, especially bioburden and endotoxin testing. Be prepared to discuss your practical experience with these techniques and how they apply to the role.
✨Familiarise Yourself with GMP Standards
Since the role is within a GMP environment, make sure you understand the principles of Good Manufacturing Practice. Be ready to explain how you've adhered to these standards in your previous roles.
✨Demonstrate Attention to Detail
This position requires a high level of accuracy and organisation. Prepare examples from your past work where your attention to detail made a significant impact on the outcome of a project or task.
✨Show Enthusiasm for Collaboration
Touchlight values teamwork, so be ready to discuss how you've successfully worked in multi-talented teams. Highlight any experiences where collaboration led to improved results in your previous roles.
