Join a business with
vision and heart

We’re calling on medical professionals, NGOs, entrepreneurs, software engineers and, of course, parents to join us as we revolutionize maternity care. Share your ideas in M-Lab or add your voice to ours in social media. We’re here to connect, support and empower.

We're a brilliant team

We’re exceptional data scientists,
software engineers and hardware designers,
bringing a touch of brilliance to everything we do

We’re empowered to innovate

We’re given ownership and independence
in a friendly, vibrant environment

We’re global

We come from diverse, multicultural backgrounds
and can grow with a well-funded global business

We want to do good

We believe that technology should be
used to genuinely benefit humankind –
especially babies and their parents

Open positions

Does Nuvo sound like the right place for a new beginning?
Take alook at the jobs below.

Site Reliability Engineer
Cloud Engineering Team Member
Full Time - Multiple

Site Reliability Engineer , Multiple

In this role as a member of the cloud engineering team, you will build and maintain global-scale, highly reliable software systems


· Design, implement and maintain cloud-native solutions using infrastructure as code methodologies

· Operate and develop micro-service containerized applications backed by cutting edge technologies

· Design, build and implement deep observability tools and methods

· Support and guide software teams on best practices and provide implementation solutions


·     Proven experience with Kubernetes and Linux containers (must)

·     At least 2 years of software development experience in Java \ C# \ Go

·     Experience with scripting languages such as bash, python

·     Experience with CI systems and Git

·     Operational, systems or networking knowledge

·     Strong passion for details and tackling complex tasks

·     Team player, fast learner and has a “get things done” attitude

Send CV’s to:

System Validation Engineer
System Validation Engineer
Full Time - Multiple

System Validation Engineer , Multiple


Create, define, develop and execute system validation tests for a multidisciplinary platform including HW & Mechanics.


  • BSc in Electrical Engineering, Mechanical Engineering or Quality Engineering
  • 5 years of experience with product validation
  • In depth understanding of multiple system areas
  • Experience leading processes with subcontractors
  • Strong written & verbal English skills
  • Experience with IQ/PQ/OQ – an advantage

Send CV’s to:

R&D Mechanical Engineer
Mechanical Engineer
Full time — Multiple

R&D Mechanical Engineer , Multiple

As a member of the Mechanical engineering team, you will be involved in the development of our medical wearable sensory system, which includes combining complex mechanics & a fabric wearable device.


  • B.Sc. in Mechanical Engineering
  • 5+ years’ experience of mechanical engineering for R&D
  • Experience with plastic material design & manufacturing, injection molding and manufacturing processes
  • Ability to work with multiple interfaces (electronic design, product design, engineering)
  • Experience writing R&D documents for medical devices – an advantage
  • Familiarity with SolidWorks
  • Experience with ePDM, Agile – advantage
  • English – fluent reading and writing
  • Multitasking – ability to manage multiple tasks effectively under tight schedule

Send CV’s to:

Technical Writer
Head of Mobile Software Development
Full time — New York
New York

Technical Writer , New York

The technical writer is responsible for providing support for R&D teams by applying professional documentation practices. The technical writer will be engaged in creating and converting an existing documentation according to FDA/CE requirements and internal standards. Deliverables include requirement documentation, verification and/or validation plans, protocols, and reports.


·     Work with R&D, regulatory and QA teams to obtain an in-depth understanding of the platform and the documentation requirements

·     Create and maintain release notes

·     Create and maintain user manuals

·     Full documentation lifecycle – create, standardize across the company, maintain continuity and consistency of style of content, revise as new issues arise


·     5+ years’ experience in Technical Writing in a regulatory environment (Medical Device preferred)

·     Experience with documentation per FDA/CE design control and ISO 13485

·     Understanding of engineering best practices and test methodologies

·     Manage multiple tasks and priorities simultaneously and adapt to changes in program priorities

·     Excellent communication and interpersonal skills

·     Excellent English language skills

Send CV’s to: