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Engineers working together at a development bench.

Careers

Build devices that reach patients.

Engineering, clinical and regulatory roles at a medical device company that designs, builds, validates and clears its own products.

Small teams, whole problems.

We do not hand work between departments. An engineer here sees a device from requirement through verification, transfer and into production, alongside the clinical and regulatory people deciding what the evidence has to prove.

That means the work is broader than a specialist role at a larger organisation, and the feedback loop from a design decision to a real consequence is much shorter.

Where we hire

The disciplines we build teams around.

Engineering

Electronics, firmware, mechanical, software and AI, plus verification and test.

Clinical research

Study design, site operations, monitoring, data management and biostatistics.

Quality and regulatory

Design controls, risk management, submissions and post-market compliance.

Manufacturing

Process engineering, production, quality control and supply chain.

How we hire

Four steps, no theatre.

01

Apply

Send a profile and a short note about the work you want to be doing.

02

Conversation

A first call about your experience and what the role actually involves.

03

Technical discussion

A working conversation with the team you would join, based on real problems rather than puzzles.

04

Offer

Scope, level and compensation discussed openly before anything is signed.

Open roles

What is open right now.

We post roles as they open. If nothing listed matches you and you work in one of the disciplines above, write to us anyway. We keep good profiles on file.

Roles are listed here as they open.

Speculative applications are read.

Based in Chennai, India.

Write to contact@rhythmrx.ai.

Next step

Want to work on this?

Send a profile and tell us which part of the device journey interests you most.