Position: Paid Internship – Part-time Location: Madrid

Publication: September 2026 Recruitment: September 2026

About us

CORIFY CARE is a start-up with the purpose of changing the paradigm of cardiac arrhythmia management. Our non-invasive cardiac mapping technology was awarded as 2020 European Innovation of the Year by the European Institute of Technology, and as the best Health Start-up in 2022 by CaixaBank EmprendeXXI.

Currently, we are looking for a highly motivated Quality and Regulatory Technician to join our team at Corify Care. The selected candidate will be responsible for supporting the control and improvement of our Quality Management System, ensuring the quality and safety of our products.

Your key responsibilities

- Collaborating in the implementation and maintenance of quality management systems, such as ISO 13485 and FDA CFR, to ensure compliance with regulatory standards. Some example duties include the management of corrective and preventive actions, the improvement of product, customer and providers traceability and the participation in post-market surveillance activities.
- Collaborating in the development, update and maintenance of technical documentation, product specifications, verification documentation, instructions for use,



and other documentation related with the regulatory compliance of medical devices.
- Participating in internal and external audits related to the quality and regulation of medical devices.
- Implementing and documenting verification of new tools and processes.

Requirements

- Recently completed or about to complete Degree in Engineering, preferably Biomedical Engineering, or related with health science.
- High level of spoken and written English.
- Good documentation and organization skills.

Soft Skills

- Ability to understand complex technologies
- Effective communication skills for collaboration with multidisciplinary teams and regulatory authorities.
- Ability to work independently with attention to detail

Valuable

- Knowledge of medical device regulations and standards, such as ISO 13485, MDR or FDA.
- Master in Engineering, preferably Biomedical Engineering, or related with health science or regulatory affairs.
- Prior experience in the medical device industry.

If are looking to contribute not only to company activity, but also to improve patients’ lives, join us

Send your CV and a cover letter by 21th September 2026 to [email protected] and we will get back to you shortly!

📌 RA/QA Specialist Intership (Madrid)
🏢 Corify
📍 Madrid