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Automating FDA compliance and approval

Jobs at Enzyme

Imagine a world in which every new piece of medical technology -- every new chemo drug, pacemaker, Alzheimer’s therapy -- gets in the hands of patients 30% faster. That’s the world we’re building. And we’re looking for people who are motivated by the idea of being a force multiplier across an industry, and thus having a small hand in every new exciting technology being developed over the next 10 years.

Enzyme is enabling the next generation of biomedical technology by building FDA approval as a service. Our software allows our customers to get their products to market faster, with less capital and less risk of getting denied by FDA. Our mission is to ensure that no product ever fails to succeed because of regulatory issues.

We’re backed by YCombinator, Refactor Capital, Data Collective and Rock Health.
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Intern - Regulatory Affairs / Quality Systems

The Regulatory Affairs / Quality Systems Technical Writer will support company growth and our product offerings with responsibility for the hands-on management of documentation supporting a variety of quality management systems with various scopes across a myriad of product types. This is an...