Posted on:November 28, 2025
Quality (QA) Lead - CDMO at Mytos
Mytos is hiring a Quality (QA) Lead - CDMO in London, UK +1 more. On-site.
About Mytos
Mytos is a contract development and manufacturing organization (CDMO) for regenerative medicine. It uses its iDEM automation technology to automate cell culture unit operations, aiming to enable scalable and consistent production at low cost per dose. The company serves clinical-stage companies and handles manufacturing from process and analytical development to regulatory support, with applications across indications such as bone fractures, deafness, and corneal blindness.
Quality (QA) Lead - CDMO job description
About Us
You rarely get the chance to change an entire industry. But that's the position we find ourselves in. Join us, and you’ll help scale cures to patients that need them sooner.
We’ve developed fully-automated cell manufacturing sites powered by custom robotics - to scale therapies to millions of patients. Last year, patients were cured of diseases like Parkinson’s and vision loss using stem-cell derived cells - but today these Regenerative Medicines are produced by hand, meaning they’re too expensive and hard to scale. With our automated CDMO, these therapies can now be scaled globally at low cost.
We've announced partnerships across multiple therapies so far ranging from Parkinson’s, to hearing loss, to bone repair - and raised $24m to expand into the market faster, and accelerate our development! Within the next 12-18 months, neurons grown on our machines will be going into Parkinson’s patient brains.
We’ve assembled a world-class team to take on this challenge, with ex-Dyson engineers and Nature-published scientists working hand-in-hand. You can learn more about your potential Mytos teammates here: Team
Mytos is backed by Y Combinator, the most successful startup program in the world which produced companies such as AirBnb, Dropbox, and Ginkgo Bioworks.
The Role
We’re looking for an ambitious and pragmatic Quality Assurance Lead to work with leadership to ensure quality moves in hand in hand with business vision. You’ll work on moving us fast towards our MHRA Manufacturing and Import Authorisation (MIA) license for our first site. You’ll get to collaborate with our advisors, such as former VP Quality for Cell and Gene Therapy at Catalent, and the former CTO of Regenerative Medicine at Resilience. This is a unique opportunity to establish quality at the world’s first automated CDMO for Regenerative Medicine.
What you'll be doing:
You bring:
Nice to have:
Salary and Benefits:
We’re building a team that enjoys moving fast, strives for continuous improvement through learning from mistakes and is passionate about work that contributes to solving real world problems.
Join us if you want a fast-paced environment, where you’re empowered to make decisions and do the best work of your career.
