At a Glance
- Tasks: Join our team to develop cutting-edge analytical tools for genetic medicine.
- Company: Touchlight is revolutionising DNA manufacturing for advanced genetic therapies.
- Benefits: Enjoy flexible working, competitive pay, and a vibrant workplace culture.
- Other info: We celebrate diversity and encourage applicants from all backgrounds.
- Why this job: Be part of a dynamic team making a real impact in the future of medicine.
- Qualifications: Bachelor’s in Biology, Biotechnology, or Biochemistry; experience in Analytical Development preferred.
The predicted salary is between 48000 - 72000 £ 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 an experienced scientist to join its Analytical Development department. This role, based at the Hampton site (UK), would be suitable for someone with a passion for development of analytical tools for solving a wide range of client specific testing requirements. The role requires a high level of communication, planning and organisation, very dynamic, and ability to thrive in a fast-paced environment, dealing with multiple stakeholders, and managing evolving priorities. The Sr Analytical Development Scientist is primarily responsible for supporting the team during all assay development activities including those required for a regulated environment, as well as participating in the sampling and testing using those analytical tools. There will be a close interaction with the other operational departments to support on-going project and product needs. The successful candidate will report directly to the Head of Analytical Development.
Key responsibilities include:
- Contribute to the hands-on development and validation of analytical assays for both internal and external programmes, in line with regulatory expectations.
- Work collaboratively with Programme Management, Quality, Supply Chain, Development, Manufacturing, and other departments, to meet deliverables and timelines.
- Ensure the organisation can deliver on a highly complex analytical testing portfolio whilst maintaining a high throughput of customer and internal projects.
- Author documentation such as standard operating procedures, validation protocols, various reports, as well as AD material ordering and storage area control.
- Participate in client meetings and support with client project communication.
- Participate and support investigations for OOS/Deviations/Change controls relating to materials coordinating with production.
- Maintain the calibration, qualification and validation of analytical testing equipment.
Skills and Experience:
- Bachelor’s Degree in one of the following fields of study: Biology, Biotechnology, Biochemistry, or equivalent experience.
- Experience working within an Analytical Development environment.
- Experience in a GMP Regulated CDMO would be beneficial.
- Experience with at least two of the listed techniques: ELISA, enzyme activity assays, qPCR/digital PCR, U/HPLC, mass spectrometry is essential.
- Knowledge of equipment and instrument calibration, qualification, and validation (UPLC, mass spectrometry, UV Spectrometry, real-time PCR/Digital PCR, Plate readers, Sanger Sequencing).
- Experience of reagent preparations and material handling.
- Advanced critical thinking and problem solving skills.
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 Analytical Development Scientist in London employer: Touchlight
Touchlight is an exceptional employer, offering a dynamic and innovative work environment at our Hampton site, where you can contribute to groundbreaking advancements in genetic medicines. We prioritise employee growth through collaborative projects, flexible working arrangements, and a competitive benefits package, all while fostering a diverse and inclusive culture that values every individual's contribution.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Analytical Development Scientist in London
✨Tip Number 1
Familiarise yourself with the latest advancements in analytical techniques relevant to the role, such as ELISA and qPCR. This will not only enhance your understanding but also allow you to engage in meaningful discussions during interviews.
✨Tip Number 2
Network with professionals in the field of analytical development, especially those working in GMP regulated environments. Attend industry conferences or webinars to make connections that could provide insights into the company culture and expectations.
✨Tip Number 3
Prepare to discuss specific examples from your past experience where you successfully developed or validated analytical assays. Highlight your problem-solving skills and ability to work collaboratively with various departments.
✨Tip Number 4
Research Touchlight’s unique DNA vector technology and its applications in genetic medicines. Being knowledgeable about their products and mission will demonstrate your genuine interest in the company and the role.
We think you need these skills to ace Senior Analytical Development Scientist in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights relevant experience in analytical development, particularly in a GMP regulated environment. Emphasise your familiarity with techniques like ELISA, qPCR, and mass spectrometry, as these are essential for the role.
Craft a Compelling Cover Letter:In your cover letter, express your passion for genetic medicines and how your skills align with Touchlight's mission. Mention specific projects or experiences that demonstrate your ability to thrive in a fast-paced environment and manage multiple stakeholders.
Showcase Communication Skills:Since the role requires high levels of communication, include examples in your application that showcase your ability to collaborate with various departments and effectively communicate project updates to clients.
Highlight Problem-Solving Abilities:Touchlight values advanced critical thinking and problem-solving skills. Provide examples in your application where you successfully navigated challenges in previous roles, particularly in analytical testing or project management.
How to prepare for a job interview at Touchlight
✨Showcase Your Technical Expertise
As a Senior Analytical Development Scientist, it's crucial to demonstrate your knowledge of analytical techniques like ELISA, qPCR, and mass spectrometry. Be prepared to discuss your hands-on experience with these methods and how you've applied them in previous roles.
✨Emphasise Collaboration Skills
This role requires working closely with various departments. Highlight your ability to collaborate effectively with Programme Management, Quality, and Manufacturing teams. Share examples of successful projects where teamwork was key to meeting deliverables.
✨Prepare for Regulatory Discussions
Since the position involves working in a regulated environment, be ready to discuss your understanding of GMP regulations and how you've ensured compliance in past projects. This will show your readiness to contribute to Touchlight's high standards.
✨Demonstrate Problem-Solving Abilities
Touchlight values critical thinking and problem-solving skills. Prepare to discuss specific challenges you've faced in analytical development and how you approached resolving them. This will illustrate your capability to thrive in a fast-paced environment.
