Build with us the future of telerehabilitation
Join DyCare and work at the intersection of artificial intelligence, computer vision, and health to transform how thousands of people experience their recovery.
Technology matters. The people who build it, matter more
Technology with purpose
You will work with computer vision, artificial intelligence, and technology applied to health to solve real clinical problems.
Impact that you can see
You will work with computer vision, artificial intelligence, and technology applied to health to solve real clinical problems.
Science + technology + people
You will work with computer vision, artificial intelligence, and technology applied to health to solve real clinical problems.
Why join the team?
Multicultural environment
Send us your CV and explain why you are interested
in the position.
Hybrid work
We combine office days in Barcelona with remote work days.
Work-life balance
Conversation with those who will be your team and
your manager
Innovation pace
If there is a match on both sides, we will make you an
offer.
Open vacancies
Management, Technical Documentation, and audits.
What do we offer?
📍 Barcelona — hybrid model
📜 Permanent contract
🚀 Professional growth in an innovative and rapidly growing environment.
As a QA/RA Specialist, you will be the guardian of compliance at DyCare. You will ensure that our products meet the highest quality standards and international regulations, allowing us to continue bringing digital rehabilitation to new markets.
What will you do at DyCare?
- You will lead the management and maintenance of our Quality Management System (QMS) certified under ISO 13485.
- You will represent Regulatory Affairs in R&D teams and communicate key regulatory changes.
- You will ensure compliance with Regulation (EU) 2017/745 (MDR) as PRRC/TR, which includes:
- The conformity of our products with the regulations.
- The technical documentation and the EU declaration of conformity.
- Post-marketing surveillance and monitoring activities.
- Notifications of serious incidents and safety corrective actions. e) Requests for health authority approvals and clinical investigations. You will manage the health registration in LATAM, USA and other jurisdictions.
- You will evaluate the impact of data processed by our products and ensure their protection.
- You will review service contracts with clients to ensure regulatory compliance.
- You will oversee advertising material to ensure it complies with regulations.
What are we looking for?
- Approximately 2–5 years of experience in QA/RA.
- Minimum B2 English.
- Studies in Law, Pharmacy, Engineering, or Life Sciences.
- Experience in international markets and LATAM/USA regulations.
- Experience preferably in Medical Devices / SaMD.
- Knowledge of EU MDR 2017/745, ISO 13485, and ISO 14971.
- Experience with is valued:
- IEC 62304, IEC 62366-1, PMS, Risk.
- GDPR (2016/679), ISO 62304, ISO 82304-1, ISO 62366-1.
- Knowledge in cybersecurity: ISO 27001 / ENS.
- Experience with is valued: