Regulatory Affairs & Compliance Associate (HealthTech)
MiMIAT Health
Who are we?
MiMIAT Health is building the patient-anchored operating system for chronic disease management.
Through a portable health data wallet, patients can bring together time-stamped Patient-Generated Health Data (PGHD), clinical records, and data from medical devices and wearables. This transforms fragmented health information into a longitudinal flow of Real-World Data that can be shared more easily across providers and geographies.
For care teams, MiMIAT provides real-time data and clinician-ready summaries that can help flag anomalies earlier, support risk stratification, and track treatment effectiveness over time.
We are currently in pilot deployments across healthcare and institutional environments, with recognition and support from leading innovation ecosystems including AstraZeneca ACCIÓN, Google Startups for Sustainable Development, and NVIDIA Inception.
Our mission? To give patients back control, reduce delays in care, and make chronic disease management more dignified, inclusive, and data-driven.
What are we looking for?
We’re looking for a Regulatory Affairs & Compliance Associate to help us strengthen MiMIAT’s regulatory and compliance foundations as we continue expanding across clinical and healthcare environments.
Given our current stage, this is an initial pro-bono collaboration with a light commitment of around 1–2 hours per week, ideal for someone who wants to contribute meaningfully to a real healthtech project without overextending themselves.
You’ll be joining a purpose-driven, fast-growing startup centered on dignity, inclusion, and patient empowerment. You will work directly with the Founder & CEO, helping us think through key regulatory and compliance questions around digital health, patient data, product positioning, and provider-facing growth.
As MiMIAT continues evolving through pilots and real-world deployments, this role will support the development of the regulatory, compliance, and ethical foundations needed to scale responsibly.
What you’ll do
- Review and help draft core documentation, including Privacy Policies, Terms & Conditions, consent flows, and other compliance-facing materials.
- Support MiMIAT in interpreting regulatory and compliance questions related to digital health, patient data, provider-facing workflows, and product evolution.
- Help think through product positioning, claims, and feature development from a regulatory perspective, including MDR-related boundary questions where relevant.
- Assess practical risks and open questions related to data flows, privacy, and healthcare operations, and help guide next steps.
- Support preparation for pilots and conversations with hospitals, clinics, and public or private healthcare stakeholders where regulatory or compliance topics may arise.
- Identify areas that require deeper external legal or specialist review, and help structure those issues clearly for escalation.
Who are you?
- You have experience or strong familiarity with GDPR, digital health regulation, health data law, regulatory affairs, or compliance in regulated environments.
- You have worked with, studied, or closely followed HealthTech, clinical research, MedTech, or other regulated innovation contexts.
- You are comfortable translating legal or regulatory requirements into practical policies, workflows, and clear recommendations.
- You can operate with sound judgment, while also knowing when an issue needs deeper specialist input.
- You can commit around 1–2 hours per week and are excited by the opportunity to contribute at a foundational stage.
- Bonus if you have familiarity with QMS concepts and standards commonly relevant in regulated environments, such as ISO 13485 or ISO/IEC 27001.
Benefits
- This is currently an initial pro-bono / unpaid collaboration (1–2 hours per week), designed for someone who believes in the mission and is excited to contribute at a foundational stage.
- The role has the potential to evolve into a formal paid position, depending on funding, scope, and mutual fit over time.
- The role offers hands-on exposure to real regulatory, compliance, and product-positioning questions inside an active HealthTech company operating across healthcare and institutional environments.
- You’ll work directly with the Founder & CEO, contributing to decisions that help shape MiMIAT’s regulatory, compliance, and ethical foundations.
- You’ll gain experience at the intersection of digital health, patient data, privacy, and real-world deployment.
- MiMIAT Health has been backed and supported by leading ecosystems including AstraZeneca ACCIÓN, Google Startups for Sustainable Development, NVIDIA Inception, and ESADE eWorks.
How to apply
Send your CV to info@mimiathealth.com or reach out directly here on LinkedIn.
If this speaks to you, we’d love to hear from you!





