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Quality Assurance Lead - CDMO

MytosLondon and Stevenage
On-site Full-time $24K/yr - $24K/yr

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Experience Level

Manager

Qualifications

Proven experience in quality assurance within a biopharmaceutical or CDMO environment. Strong understanding of regulatory requirements and quality standards related to cell and gene therapies. Ability to lead and inspire cross-functional teams in a fast-paced environment. Excellent communication skills, both written and verbal. Experience with MHRA and EMA regulations is highly desirable.

About the job

About Us
At Mytos, we are at the forefront of transforming the healthcare industry. Join our mission to expedite the delivery of life-saving therapies to patients in need.

Our state-of-the-art, fully automated cell manufacturing facilities utilize customized robotics to produce regenerative therapies at scale. Recently, we have successfully treated patients suffering from conditions such as Parkinson’s and vision impairments using stem-cell derived treatments. However, the current manual production methods hinder scalability and affordability. With our innovative CDMO solutions, we aim to make these therapies accessible globally.

We have established several partnerships across diverse therapeutic areas including Parkinson’s, hearing loss, and bone repair, and we have successfully raised $24 million to accelerate our market entry and development efforts! Within the next year, we anticipate our neuron production technology will be implemented in treatments for Parkinson’s patients.

Our team is comprised of top-tier talent, including former engineers from Dyson and scientists published in prestigious journals. To learn more about your potential colleagues at Mytos, visit: Team

Mytos is proud to be backed by Y Combinator, the world's most successful startup accelerator, known for launching companies like Airbnb, Dropbox, and Ginkgo Bioworks.

The Role
We are seeking a driven and practical Quality Assurance Lead to collaborate with our leadership team, ensuring that quality aligns with our business objectives. You will play a pivotal role in our journey towards obtaining the MHRA Manufacturing and Import Authorisation (MIA) for our initial facility. This position offers the unique chance to work alongside industry experts, including a former VP of Quality for Cell and Gene Therapy at Catalent and the former CTO of Regenerative Medicine at Resilience. This is an exceptional opportunity to establish a culture of quality at Mytos.

About Mytos

Mytos is revolutionizing the biopharmaceutical industry with automated solutions for cell manufacturing, enabling scalable and affordable regenerative therapies. Our innovative technology aims to change the way diseases are treated, making advanced therapies accessible to millions of patients worldwide.

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